A compound of formula (I)
##STR00001##
Wherein x, Y, ring A, ring b, l, m, R1, R2, R4 and R5 are as defined herein, to supress intracellular signal transduction or cell activation induced by endotoxin and to suppress cell responses due to the intracellular signal transduction and cell activation such as an excess generation of inflammatory mediators such as TNF-α, pharmacologically acceptable salts therefor, a preparation method therefor, and a medicament containing the aforementioned substituted cycloalkene derivative as an active ingredient which is superior in prophylaxis and/or treatment of diseases such as sepsis (septic shock, disseminated intravascular coagulation, multiple organ failure and the like), that are associated with intracellular signal transduction or cell activation induced by endotoxin and to cell responses to the intracellular signal transduction and cell activation.
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35. A potassium salt of ethyl (2R,3R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate.
41. potassium (2-chloro-4-fluorophenyl){[(2R,3R,8R)-7-(ethoxycarbonyl)-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-en-8-yl] sulfonyl}azanide.
34. A pharmaceutically acceptable salt of ethyl (2R,3R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate.
40. A pharmaceutically acceptable salt of ethyl (2R,3R,8R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4dioxaspiro[4.5]dec-6-ene-7-carboxylate.
##STR00204##
{wherein
x and Y represent a group in which x and Y together with the carbon atom of ring b to which they are bound form ring A, or x and Y together represent a substituent of ring b, or x and Y each represents a hydrogen atom;
(1) in the case where x and Y represent a group in which x and Y together with the carbon atom of ring b to which they are bound form ring A:
ring A represents
a 3- to 7-membered heterocyclyl ring (in the heterocyclyl ring, x and Y, independently from each other, represent any one selected from a carbon atom, a group having the formula nr (R represents a hydrogen atom or a c1-c6 alkyl, c2-c6 alkenyl, c2-c6 alkynyl or c1-c6 alkanoyl group which may be substituted with one or more groups selected from substituent group α), an oxygen atom, a sulfur atom, a group having the formula SO and a group having the formula SO2, the heterocyclyl ring may include an unsaturated bond,
may form a fused ring or spiro ring with a 3- to 7-membered heterocyclyl ring or 3- to 7-membered cycloalkyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with the same or different 1 to 4 groups selected from the group consisting of an oxo group, a thioxo group, substituent group α, a cyclopropyl c1-c6 alkyl group,
a c1-c6 alkyl group which may be substituted with 1 to 5 groups selected from substituent group α,
a c2-c6 alkenyl group which may be substituted with 1 to 5 groups selected from substituent group α, and a c2-c6 alkynyl group which may be substituted with 1 to 5 groups selected from substituent group α) or
a 3- to 7-membered cycloalkyl ring (the cycloalkyl ring may include an unsaturated bond, may form a fused ring or spiro ring with a 3- to 7-membered heterocyclyl ring or 3- to 7-membered cycloalkyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with the same or different 1 to 4 groups selected from the group consisting of substituent group α, a cyclopropyl c1-c6 alkyl group,
a c1-c6 alkyl group which may be substituted with 1 to 5 groups selected from substituent group α,
a c2-c6 alkenyl group which may be substituted with 1 to 5 groups selected from substituent group α, and
a c2-c6 alkynyl group which may be substituted with 1 to 5 groups selected from substituent group α);
(2) in the case where x and Y together represent a substituent of ring b:
x and Y represent an oxo group or a thioxo group;
1 and m, independently from each other, represent an integer of 0 to 3, and 1+m is 1 to 3;
R1 represents
an aliphatic hydrocarbon group which may be substituted with one or more groups selected from substituent group β and substituent group γ (wherein the aliphatic hydrocarbon group represents a c1-c20 alkyl group, c3-c10cycloalkyl group, c4-c12 cycloalkylalkyl group, c3-c6 alkenyl group or c3-c6 alkynyl group),
a phenyl group which may be substituted with one or more groups selected from substituent group δ,
a group having the formula OR4 (R4 represents a hydrogen atom or an aliphatic hydrocarbon group which may be substituted with one or more groups selected from substituent group β and substituent group γ, the aliphatic hydrocarbon group has the same meaning as defined above) or a halogen atom;
n represents an integer of 0 to 3;
R2 represents a hydrogen atom,
a c1-c6 alkyl group which may be substituted with one or more groups selected from substituent group β,
a c2-c6 alkenyl group which may be substituted with one or more groups selected from substituent group β, or
a c2-c6 alkynyl group which may be substituted with one or more groups selected from substituent group β;
R3 represents
a phenyl group which may be substituted with one or more groups selected from substituent group ε, or
a 5- or 6-membered heteroaryl group which may be substituted with one or more groups selected from substituent group ε (the heteroaryl group includes 1 to 3 hetero atoms selected from a nitrogen atom, oxygen atom and sulfur atom);
R5 represents a hydrogen atom,
a c1-c6 alkyl group which may be substituted with one or more groups selected from substituent group β,
a c2-c6 alkenyl group which may be substituted with one or more groups selected from substituent group β, or
a c2-c6 alkynyl group which may be substituted with one or more groups selected from substituent group β;
provided that in the case where R3 is a phenyl group which may be substituted with one or more groups selected from substituent group ε, x and Y represent the aforementioned (1) or (2);
substituent group α represents
a hydroxy group, halogen atom, c1-c6 alkoxy group, halogeno c1-c6 alkoxy group, carboxy group, c1-c6 alkoxy-carbonyl group;
carbamoyl group which may be substituted with one or more groups selected from a c1-c6 alkyl group, c2-c6 alkenyl group, c2-c6 alkynyl group, c1-c6 alkanoyl group or c2-c6 alkenyl-carbonyl group;
and a group having the formula nr6R7, and
R6 and R7, independently from each other, represent a hydrogen atom, c1-c6 alkyl group, c2-c6 alkenyl group, c2-c6 alkynyl group, c1-c6 alkanoyl group or c2-c6 alkenyl-carbonyl group, or together with the nitrogen atom to which they are bound form a heterocyclyl group;
substituent group β represents
an oxo group, hydroxy group, cyclopropyl group, c1-c6 alkoxy group, c1-c6 alkylthio group, nitro group, halogen atom, cyano group, carboxy group, c1-c10 alkoxy-carbonyl group, c1-c6 alkanoyl group, c2-c4 alkenyl-carbonyl group, c2-c6 alkanoyloxy group, c2-c4 alkenyl-carbonyloxy group;
carbamoyl group which may be substituted with one or more groups selected from a c1-c4 alkyl group, phenyl group, c1-c7 acyl group and c1-c4 alkoxy-phenyl group;
thiocarbamoyl group which may be substituted with a c1-c4 alkyl group or phenyl group;
carbamoyloxy group which may be substituted with a c1-c4 alkyl group or phenyl group;
c1-c6 alkanoylamino group, c1-c10 alkoxy-carboxamide group, c1-c10 alkoxy-carbonyloxy group, and
ureido group which may be substituted with a c1-c4 alkyl group or phenyl group;
substituent group γ represents
a heterocyclic group, c3-c10 cycloalkyloxy group, c6-c10 aryloxy group, c7-c19 aralkyloxy group, heterocyclyloxy group, c3-c10 cycloalkylthio group, c6-c10 arylthio group, c7-c19 aralkylthio group, heterocyclylthio group, heterocyclylsulfinyl group, heterocyclylsulfonyl group, c3-c6 cycloalkyloxy-carbonyl group, c6-c10 aryloxy-carbonyl group, c7-c19 aralkyloxy-carbonyl group, heterocyclyloxycarbonyl group, c6-c10aryl-carbonyl group, c6-c10 aryl-carbonyloxy group, c6-c10 aryl-carbonylamino group, c6-c10 aryloxy-carboxamide group, c7-c19 aralkyloxy-carboxamide group, c6-c10 aryloxy-carbonyloxy group, c7-c19 aralkyloxy-carbonyloxy group, c3-c10 cycloalkyloxy-carbonyloxy group and c6-c10 aryl group which may be substituted with one or more groups selected from substituent group β;
substituent group δ represents
a hydroxy group, nitro group, cyano group, halogen atom, c1-c6 alkyl group, halogeno c1-c6 alkyl group, c1-c6 alkoxy group, halogeno c1-c6 alkoxy group, carboxy group, c1-c6 alkanoyl group, c1-c6 alkoxy-carbonyl group, c1-c6 alkanoylamino group, c1-c6 alkylthio group, carbamoyl group, c1-c6 alkyl-carbamoyl group, c1-c6 alkoxy-carbonyl c1-c6 alkyl-carbamoyl group, 1,3-diacylguanidino c1-c6 alkyl group, a group having the formula nr6R7 (R6 and R7 are the same as R6 and R7 of substituent group α), c3-c6 cycloalkyl group, c6-c10 aryl group and 5-membered heteroaryl group; and
substituent group ε represents
a hydroxy group, nitro group, cyano group, halogen atom, c1-c14 alkyl group, cyclopropyl c1-c14 alkyl group, halogeno c1-c14 alkyl group, c1-c14 alkoxy group, halogeno c1-c14 alkoxy group, carboxy group, c1-c14 alkanoyl group, c1-c14 alkoxy-carbonyl group, c1-c14 alkanoylamino group, c1-c14 alkylthio group, carbamoyl group, c1-c14 alkyl-carbamoyl group, c1-c14 alkoxy-carbonyl c1-c14 alkyl-carbamoyl group, 1,3-diacylguanidino c1-c14 alkyl group, group having the formula nr6R7 (R6 and R7 are the same as R6 and R7 of substituent group α), c3-c6 cycloalkyl group, c6-c10 aryl group and 5-membered heteroaryl group} or a pharmacologically acceptable salt thereof.
2. The compound or pharmacologically acceptable salt thereof according to
3. The compound or pharmacologically acceptable salt thereof according to
4. The compound or pharmacologically acceptable salt thereof according to
x and Y together with the carbon atom of ring b form ring A, and ring A is a 3- to 7-membered heterocyclyl ring
(in the heterocyclyl ring, x and Y, independently from each other, represent any one selected from a carbon atom, a group having the formula nr (R represents a hydrogen atom or a c1-c6 alkyl, c2-c6 alkenyl, c2-c6 alkynyl or c1-c6 alkanoyl group which may be substituted with one or more groups selected from substituent group α), an oxygen atom, a sulfur atom, a group having the formula SO and a group having the formula SO2,
the heterocyclyl ring may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the heterocyclyl ring includes 1 or 2 oxygen and/or nitrogen atoms as hetero atoms) or 5- to 6-membered cycloalkyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with the same or different 1 to 4 groups selected from the group consisting of an oxo group, a thioxo group, substituent group α, a cyclopropyl c1-c6 alkyl group and a c1-c6 alkyl group which may be substituted with 1 to 5 groups selected from substituent group α) or
a 3- to 7-membered saturated cycloalkyl ring
(the 3- to 7-membered saturated cycloalkyl ring may be substituted with 1 or 2 groups selected from the group consisting of a hydroxy group, hydroxymethyl group, 1,2-dihydroxyethyl group, 1,2,3-trihydroxypropyl group, 1,2,3,4-tetrahydroxybutyl group and acetylamino group).
5. The compound or pharmacologically acceptable salt thereof according to
x and Y represent a group in which x and Y together with the carbon atom of ring b form ring A, and ring A is
a 3- to 7-membered heterocyclyl ring
(in the heterocyclyl ring, x and Y, independently from each other, represent any one selected from a carbon atom, an oxygen atom, sulfur atom, a group having the formula SO and a group having the formula SO2,
the heterocyclyl ring may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the heterocyclyl ring includes 1 or 2 oxygen and/or nitrogen atoms as hetero atoms) or 5- or 6-membered cycloalkyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with the same or different 1 to 4 groups selected from the group consisting of an oxo group, a thioxo group, substituent group α and a c1-c6 alkyl group which may be substituted with 1 to 4 groups selected from substituent group α) or
a 3- to 5-membered saturated cycloalkyl ring
(the 3- to 5-membered saturated cycloalkyl ring may be substituted with 1 or 2 groups selected from the group consisting of a hydroxymethyl group, 1,2-dihydroxyethyl group, 1,2,3-trihydroxypropyl group, 1,2,3,4-tetrahydroxybutyl group and acetylamino group).
6. The compound or pharmacologically acceptable salt thereof according to
x and Y represent a group in which x and Y together with the carbon atom of ring b form ring A, and ring A is
a 3- to 7-membered heterocyclyl ring
(the 3- to 7-membered heterocyclyl ring is oxirane, oxolane, tetrahydrofuran, tetrahydropyran, 1,3-dioxolane, 1,3-dioxane, 1,3-dioxepane, 1,3-dithiolane, 1,3-dithiane, 1,1,3,3-tetraoxo-1,3-dithiolane, 1,3-oxathiolane, 1,3-oxathiane or 1,3-oxathiepane,
these heterocyclyl rings may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the 5- or 6-membered heterocyclyl ring is tetrahydrofuran, tetrahydropyran, pyrrolidine, piperidine or 1,3-dioxane) or cyclohexyl ring, and
ring A, including the fused ring and spiro ring, may be substituted with 1 or 2 groups selected from the group consisting of an oxo group, a thioxo group, substituent group α (substituent group α represents a hydroxy group and a group having the formula nr6R7, and R6 and R7, independently from each other, represent a hydrogen atom or c1-c6 alkanoyl group), a methyl group, an ethyl group and a c1-c6 alkyl group which is substituted with 1 to 4 hydroxy groups), or
a cyclopropyl or cyclopentyl ring
(the cyclopropyl or cyclopentyl ring may be substituted with 1 or 2 groups selected from the group consisting of a hydroxymethyl group, 1,2-dihydroxyethyl group, 1,2,3-trihydroxypropyl group, and a 1,2,3,4-tetrahydroxybutyl group).
7. The compound or pharmacologically acceptable salt thereof according to
x and Y represent a group in which x and Y together with the carbon atom of ring b form ring A, and ring A is
a 3- to 6-membered heterocyclyl ring
{the heterocyclyl ring is
oxirane, tetrahydrofuran,
1,3-dioxolane, 1,3-dioxane,
1,3-dithiolane, 1,3-dithiane,
1,3-oxathiolane, or 1,3-oxathiane,
these heterocyclyl rings may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the 5- or 6-membered heterocyclyl ring is tetrahydrofuran, tetrahydropyran or 1,3-dioxane) or cyclohexyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with 1 or 2 groups selected from the group consisting of substituent group α (substituent group α represents a hydroxy group and a group having the formula nr6R7 (R6 and R7, independently from each other, represent a hydrogen atom or acetyl group), a methyl group, an ethyl group, a hydroxymethyl group, a 1,2-dihydroxyethyl group, a 1,2,3-trihydroxypropyl group and a 1,2,3,4-tetrahydroxybutyl group}.
8. The compound or pharmacologically acceptable salt thereof according to
n is 0 or 1, and
R1 is a hydroxy group, halogen atom, c1-c6 alkyl group or c1-c6 alkoxy group.
9. The compound or pharmacologically acceptable salt thereof according to
n is 0 or 1, and
R1 is a fluorine atom or methyl group.
11. The compound or pharmacologically acceptable salt thereof according to
12. The compound or pharmacologically acceptable salt thereof according to
13. The compound or pharmacologically acceptable salt thereof according to
14. The compound or pharmacologically acceptable salt thereof according to
R3 is
a phenyl group which may be substituted with one or more groups selected from substituent group ε, or
a pyrrolyl group which may be substituted with one or more groups selected from substituent group ε, and
substituent group ε is a halogen atom, c1-c14 alkyl group and halogeno c1-c14 alkyl group.
15. The compound or pharmacologically acceptable salt thereof according to
R3 is
a phenyl group which may be substituted with one or more groups selected from substituent group ε, or
a pyrrolyl group which may be substituted with one or more groups selected from substituent group ε, and
substituent group ε is a fluorine atom, chlorine atom, bromine atom, c3-c8 alkyl group and halogeno c4-c8 alkyl group.
16. The compound or pharmacologically acceptable salt thereof according to
R3 is
a phenyl group which may be substituted with one or more groups selected from substituent group ε, and
substituent group ε is a fluorine atom, chlorine atom and c3-c8 alkyl group.
17. The compound or pharmacologically acceptable salt thereof according to
18. The compound or pharmacologically acceptable salt thereof according to
19. The compound or pharmacologically acceptable salt thereof according to
20. The compounds of the following group selected from
ethyl 8-[N-(2-chloropheny)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloropheny)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2,4-difluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2,4-difluorophenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2-hydroxymethyl-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluoropheny)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluoropheny)sulfamoyl]-2-(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2-(1,2,3-trihydroxypropyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2-(1,2,3,4-tetrahydroxybutyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(acetylaminomethyl)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 9-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3-hydroxy-1,5-dioxaspiro[5.5]undec-7-ene-8-carboxylate,
ethyl 3-acetylamino-9-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,5-dioxaspiro[5.5]undec-7-ene-8-carboxylate,
ethyl 9-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-bis(hydroxymethyl)-1,5-dioxaspiro[5.5]undec-7-ene-8-carboxylate,
ethyl 8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-butyl-4-fluoropheny)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-hexylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-hexylphenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(1,2-dihydroxyethyl)-8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-heptylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-heptylphenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-heptylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(1,2-dihydroxyethyl)-8-[N-(4-fluoro-2-heptylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-bromophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-bromophenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-6-methylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-6-methylphenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(hydroxymethyl)-8-[N-(2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(1,2-dihydroxyethyl)-8-[N-(2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(1,2-dihydroxyethyl)-8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-octylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(1,2-dihydroxyethyl)-8-[N-(4-fluoro-2-octylphenyl)sulfamoyl]-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-propylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate,
ethyl 2,3-bis(1,2-dihydroxyethyl)-8-[N-(4-fluoro-2-propylphenyl)sulfamoyl]-1,4-dioxaspiro [4.5]dec-6-ene-7-carboxylate, and
ethyl 8-[N-(2-chloro-4-fluorophenyl)-N-methylsulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate.
21. A pharmaceutical composition or pharmacologically acceptable salt thereof comprising any of the compounds according to
22. A method for suppressing intracellular signal transduction or cell activation induced by, endotoxin comprising the administration of an effective amount of the pharmaceutical composition or pharmaceutically acceptable salt thereof according to
23. A method for suppressing the generation of inflammatory mediators due to intracellular signal transduction or cell activation induced by endotoxin comprising the administration of an effective amount of the pharmaceutical composition or pharmaceutically acceptable salt thereof according to
24. A method for treatment of sepsis comprising the administration of an effective amount of the pharmaceutical composition or pharmaceutically acceptable salt thereof according to
25. The compounds of the following group selected from
ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-2,3-bis(1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate,
ethyl 8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate, and
ethyl 2,3-bis(1,2-dihydroxyethyl)-8[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate.
26. The following compound selected from
27. The following compound selected from
28. The following compound selected from
29. The following compound selected from
30. The following compound selected from
31. The following compound selected from
32. The following compound selected from
33. The following compound selected from
36. A pharmaceutical composition comprising the compound according to
37. A method for treating sepsis comprising administering a pharmaceutical composition comprising the compound according to
38. A pharmaceutical composition comprising the compound according to
39. A method of treating sepsis comprising administering a pharmaceutical composition comprising the compound according to
42. A pharmaceutical composition comprising the compound according to
43. A method for treating sepsis comprising administering a pharmaceutical composition comprising the compound according to
44. A pharmaceutical composition comprising the compound according to
45. A method for treating sepsis comprising administering a pharmaceutical composition comprising the compound according to
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This Application is a Section 371 National Stage Application of International Application No. PCT/JP2006/318103, filed 13 Sep. 2006 and published as WO 2007/032362 A1 on 22 Mar. 2007, which claims the priority from the Japanese application 2005-267504, filed 14 Sep. 2005, the subject matter of which are hereby incorporated by reference in its entirety.
The present invention relates to a novel compound which has an action to suppress intracellular signal transduction or cell activation in various cells such as monocytes, macrophages and vascular endothelial cells, the intracellular signal transduction or cell activation being induced by endotoxin, and to suppress the generation of inflammatory mediators such as TNF-α due to the intracellular signal transduction and cell activation, and which is useful as a prophylactic and/or therapeutic agent for various diseases such as sepsis (septic shock, disseminated intravascular coagulation, multiple organ failure and the like), a production method therefor and a use thereof.
Sepsis is a systemic inflammatory response syndrome (SIRS) which occurs due to an excess inflammatory response of a biological body against bacterial infection, and is a disease which may result in death when it is accompanied by shock or organ failure. Since there are only a few agents that are effective against sepsis until now, it is considered to be a disease that is difficult to prevent and treat. However, since its fatality is high and the number of patients is large, development of therapeutic agents for it is particularly important (for example, refer to Non-patent document 1).
Endotoxin (lipopolysaccharide, LPS), which is a membrane component of bacteria, acts against cells such as monocytes, macrophages and vascular endothelial cells, induces an excess generation of various inflammatory mediators such as TNF-α and the like, causes sudden blood pressure reduction, blood coagulation disorders, cardiovascular disturbances and the like in addition to systemic inflammatory responses, and thus exhibits sepsis (for example, refer to Non-patent document 2). Lipid A, which corresponds to lipopolysaccharide and its partial structure, activates intracellular signal transduction via TLR4 (Toll-like receptor 4), which is a functional cell surface receptor, after binding with CD14 (for example, refer to Non-patent document 3). Accordingly, lipid A initiates various cell responses represented by the generation of inflammatory mediators. Therefore, it is considered that a substance which suppresses the intracellular signal transduction or cell activation induced by endotoxin, and various cell responses induced by intracellular signal transduction and cell activation, the various cell responses being represented by an excess generation of inflammatory mediators such as TNF-α, can be an effective prophylactic and therapeutic agent for sepsis (for example, refer to Non-patent document 3, Non-patent document 4, Patent document 1 and Patent document 2).
Intracellular signal transduction or cell activation induced by endotoxin, and various cell responses induced by the intracellular signal transduction and cell activation, the various cell responses being represented by an excess generation of inflammatory mediators such as TNF-α, lead to development and progress of various diseases such as ischemic brain disorder, arteriosclerosis, poor prognosis after coronary angioplasty, heart failure, diabetes, diabetic complication, joint inflammation, osteoporosis, osteopenia, autoimmune disease, tissue disorder and rejection after organ transplantation, bacterial infection, virus infection, gastritis, pancreatitis, nephritis, pneumonia, hepatitis and leukemia, in addition to the aforementioned sepsis (for example, Non-patent document 5 and Patent document 3).
Therefore, a substance which suppresses intracellular signal transduction or cell activation induced by endotoxin, and various cell responses induced by the intracellular signal transduction and cell activation such as an excess generation of inflammatory mediators such as TNF-α, is considered to be effective as a prophylactic and/or therapeutic agent for these various diseases, and thus the development of an excellent therapeutic agent has been desired.
As a result of conducting extensive studies on the pharmacological activity of various substituted cycloalkene derivatives for the purpose of developing a compound which has an activity to suppress intracellular signal transduction or cell activation in various cells such as monocytes, macrophages and vascular endothelial cells, the intracellular signal transduction or the cell activation being induced by endotoxin, and to suppress various cell responses induced by the intracellular signal transduction and cell activation, such as an excess generation of inflammatory mediators such as TNF-α, the inventors of the present invention found that a substituted cycloalkene derivative having a unique structure possesses an excellent suppressing effect against intracellular signal transduction or cell activation induced by endotoxin, and against cell responses induced by the intracellular signal transduction and cell activation, such as an excess generation of inflammatory mediators such as TNF-α, and found that it is useful as a prophylactic and/or therapeutic agent for various diseases such as sepsis which are associated with intracellular signal transduction or cell activation induced by endotoxin, and with cell responses induced by the intracellular signal transduction and the cell activation, thereby leading to completion of the present invention.
The present invention provides a substituted cycloalkene derivative which possesses an activity to suppress intracellular signal transduction or cell activation induced by endotoxin, and cell responses due to the intracellular signal transduction and cell activation such as an excess generation of inflammatory mediators such as TNF-α, pharmacologically acceptable salts thereof, a production method therefor, and a medicament containing the aforementioned substituted cycloalkene derivative as an active ingredient, which is excellent for prophylaxis and/or treatment of various diseases caused by intracellular signal transduction or cell activation induced by endotoxin, and caused by cell responses including an excess generation of inflammatory mediators such as TNF-α, the cell responses being induced by the intracellular signal transduction and cell activation.
Accordingly, the present invention provides:
(1) A compound represented by the general formula (I):
##STR00002##
{wherein
X and Y represent a group in which X and Y together with the carbon atom of ring B to which they are bound form ring A, X and Y together represent a substituent of ring B, or X and Y each represents a hydrogen atom.
a 3- to 7-membered heterocyclyl ring [in the heterocyclyl ring, X and Y, independently from each other, represent any one selected from a carbon atom, a group having the formula NR (R represents a hydrogen atom or a C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C1-C6 alkanoyl group which may be substituted with a group selected from Substituent group α), an oxygen atom, a sulfur atom, a group having the formula SO and a group having the formula SO2,
(2) The compound or pharmacologically acceptable salt thereof according to the aforementioned (1), wherein l is 0 and m is an integer of 1 to 3,
(3) The compound or pharmacologically acceptable salt thereof according to the aforementioned (1), wherein l is 0 and m is 2,
(4) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (3), wherein
the heterocyclyl ring may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the heterocyclyl ring includes 1 or 2 oxygen and/or nitrogen atoms as hetero atoms) or 5- or 6-membered cycloalkyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with the same or different 1 to 4 groups selected from the group consisting of an oxo group, a thioxo group, Substituent group α, a cyclopropyl C1-C6 alkyl group and a C1-C6 alkyl group which may be substituted with 1 to 5 groups selected from Substituent group α]
or
(5) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (3), wherein
(6) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (3), wherein
these heterocyclyl rings may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the 5- or 6-membered heterocyclyl ring is tetrahydrofuran, tetrahydropyran, pyrrolidine, piperidine or 1,3-dioxane) or cyclohexyl ring, and
ring A, including the fused ring or spiro ring, may be substituted with 1 or 2 groups selected from the group consisting of an oxo group, a thioxo group, Substituent group α (Substituent group α represents a hydroxy group and a group having the formula NR6R7, and R6 and R7, independently from each other, represent a hydrogen atom or C1-C6 alkanoyl group), a methyl group, an ethyl group and a C1-C6 alkyl group which is substituted with 1 to 4 hydroxy groups],
or
(7) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (3), wherein
ring A, including the fused ring and spiro ring, may be substituted with 1 or 2 groups selected from the group consisting of Substituent group α [Substituent group α represents a hydroxy group and a group having the formula NR6R7 (R6 and R7, independently from each other, represent a hydrogen atom or acetyl group)], a methyl group, an ethyl group, a hydroxymethyl group, a 1,2-dihydroxyethyl group, a 1,2,3-trihydroxypropyl group and a 1,2,3,4-tetrahydroxybutyl group},
(8) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (7), wherein
n is 0 or 1, and
R1 is a hydroxy group, halogen atom, C1-C6 alkyl group or C1-C6 alkoxy group,
(9) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (7), wherein
n is 0 or 1, and
R1 is a fluorine atom or methyl group,
(10) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (7), wherein n is 0,
(11) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (10), wherein R2 is a C1-C6 alkyl group,
(12) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (10), wherein R2 is a C1-C4 alkyl group,
(13) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (10), wherein R2 is an ethyl group,
(14) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (13), wherein
R3 is
a phenyl group which may be substituted with a group selected from Substituent group ε, or
a pyrrolyl group which may be substituted with a group selected from Substituent group ε, and
Substituent group ε is a halogen atom, C1-C14 alkyl group and halogeno C1-C14 alkyl group,
(15) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (13), wherein
R3 is
a phenyl group which may be substituted with a group selected from Substituent group ε, or
a pyrrolyl group which may be substituted with a group selected from Substituent group ε, and
Substituent group ε is a fluorine atom, chlorine atom, bromine atom, C3-C8 alkyl group and halogeno C4-C8 alkyl group,
(16) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (13), wherein
R3 is
a phenyl group which may be substituted with a group selected from Substituent group ε, and
Substituent group ε is a fluorine atom, chlorine atom and C3-C8 alkyl group,
(17) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (16), wherein R5 is a hydrogen atom or C1-C6 alkyl group,
(18) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (16), wherein R5 is a hydrogen atom or methyl group,
(19) The compound or pharmacologically acceptable salt thereof according to any one of the aforementioned (1) to (16), wherein R5 is a hydrogen atom,
(20) The compounds of the following group selected from the aforementioned (1) or pharmacologically acceptable salt thereof:
(21) A medicament containing the compound or pharmacologically acceptable salt thereof selected from any one of the aforementioned (1) to (20) as an active ingredient,
(22) The medicament according to the aforementioned (21) for use in suppressing intracellular signal transduction or cell activation induced by endotoxin,
(23) The medicament according to the aforementioned (21) for use in suppressing the generation of inflammatory mediators due to intracellular signal transduction or cell activation induced by endotoxin,
(24) The medicament according to the aforementioned (21) for use as a prophylactic or therapeutic agent for a disease due to intracellular signal transduction or cell activation inducted by endotoxin,
(25) The medicament according to the aforementioned (21) for use as a prophylactic and/or therapeutic agent for a disease mediated by an inflammatory mediator, of which generation is induced by endotoxin,
(26) The medicament according to the aforementioned (21) for use as a prophylactic and/or therapeutic agent for a disease mediated by an inflammatory mediator, which is generated due to intracellular signal transduction or cell activation induced by endotoxin,
(27) The medicament according to the aforementioned (21) for use as a prophylactic and/or therapeutic agent for sepsis, and
The substituted cycloalkene derivative according to the present invention having the general formula (I) has excellent activity to suppress intracellular signal transduction or cell activation induced by endotoxin and to suppress excess generation of inflammatory mediators such as TNF-α due to the intracellular signal transduction and cell activation, and is useful as a medicament, especially as a prophylactic and/or therapeutic agent for ischemic brain disorder, arteriosclerosis, poor prognosis after coronary angioplasty, heart failure, diabetes, diabetic complication, joint inflammation, osteoporosis, osteopenia, sepsis, autoimmune disease, tissue disorder and rejection after organ transplantation, bacterial infection, virus infection, gastritis, pancreatitis, nephritis, pneumonia, hepatitis, leukemia and the like, which are induced by the intervention of the intracellular signal transduction or cell activation, and by inflammatory mediators due to the intracellular signal transduction and cell activation.
“Halogen atom” in the definitions of R1, Substituent group α, Substituent group β, Substituent group δ and Substituent group ε includes, for example, a fluorine atom, chlorine atom, bromine atom or iodine atom.
With respect to R1, it is preferably a fluorine atom or chlorine atom, more preferably a fluorine atom.
With respect to Substituent group ε, it is preferably a fluorine atom, chlorine atom or bromine atom, more preferably a fluorine atom or chlorine atom.
“Alkyl group” in the definitions of the NR group which may be included in ring A, substituent of ring A, R1, R2, R5, R6, R7, Substituent group β, Substituent group δ and Substituent group ε includes a linear or branched alkyl group.
“C1-C6 alkyl group” of “C1-C6 alkyl group which may be substituted with a group selected from Substituent group α” in the definition of the NR group which may be included in ring A; “C1-C6 alkyl group” of “cyclopropyl C1-C6 alkyl group” in the definition of a substituent of ring A; “C1-C6 alkyl group” of “C1-C6 alkyl group which may be substituted with 1 to 5 groups selected from Substituent group α” in the definition of a substituent of ring A; “C1-C6 alkyl group” of “C1-C6 alkyl group which may be substituted with a group selected from Substituent group β” in the definitions of R2 and R5; and “C1-C6 alkyl group” in the definitions of Substituent group δ, R6 and R7 are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, 2-methylbutyl, neopentyl, 1-ethylpropyl, n-hexyl, isohexyl, 4-methylpentyl, 3-methylpentyl, 2-methylpentyl, 1-methylpentyl, 3,3-dimethylbutyl, 2,2-dimethylbutyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,3-dimethylbutyl, 2-ethylbutyl group or the like.
Among the “C1-C6 alkyl groups”, the one with respect to the NR group which may be included in ring A is preferably methyl.
With respect to a substituent of ring A, it is preferably a C1-C4 alkyl group.
With respect to R2, it is preferably a C1-C4 alkyl group, more preferably ethyl.
With respect to R5, it is preferably methyl.
With respect to R6 and R7, it is preferably methyl.
With respect to Substituent group δ, it is preferably a C1-C4 alkyl group.
C1-C14 alkyl groups of “C1-C14 alkyl group” and “cyclopropyl C1-C14 alkyl group” in the definition of Substituent group ε are, for example, the aforementioned “C1-C6 alkyl group”, octyl, nonyl, decyl, dodecyl, tetradecyl or the like.
With respect to “C1-C14 alkyl group” in the definition of Substituent group ε, it is preferably C3-C8 alkyl group.
“C1-C20 alkyl group” in the definition of R1 is, for example, the aforementioned “C1-C14 alkyl group”, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, icosyl or the like. Preferably, it is a C1-C6 alkyl group, and more preferably a methyl group.
“Alkenyl group” in the definitions of the NR group which may be included in ring A, substituent of ring A, R1, R2, R5, R6, R7 and Substituent group α is a linear or branched alkenyl group.
“C3-C6 alkenyl group” in the definition of R1 is, for example, 2-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-ethyl-2-propenyl, 2-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 1-ethyl-2-butenyl, 3-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 1-ethyl-3-butenyl, 2-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 4-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl or 5-hexenyl, preferably a C3-C4 alkenyl group.
“C2-C6 alkenyl group” of “C2-C6 alkenyl group which may be substituted with a group selected from Substituent group α” in the definition of the NR group which may be included in ring A; “C2-C6 alkenyl group” of “C2-C6 alkenyl group which may be substituted with 1 to 5 groups selected from Substituent group α” in the definition of substituent of ring A; “C2-C6 alkenyl group” of “C2-C6 alkenyl group which may be substituted with a group selected from Substituent group β” in the definitions of R2 and R5; and “C2-C6 alkenyl group” in the definitions of R6 and R7 are, for example, vinyl or the aforementioned “C3-C6 alkenyl group”, preferably a C3-C4 alkenyl group.
“Alkynyl group” in the definitions of the NR group which may be included in ring A, substituent of ring A, R1, R2, R5, R6, R7 and Substituent group α is a linear or branched alkynyl group.
“C3-C6 alkynyl group” in the definition of R1 is, for example, 2-propynyl, 1-methyl-2-propynyl, 2-butynyl, 1-methyl-2-butynyl, 1-ethyl-2-butynyl, 3-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1-ethyl-3-butynyl, 2-pentynyl, 1-methyl-2-pentynyl, 3-pentynyl, 1-methyl-3-pentynyl, 2-methyl-3-pentynyl, 4-pentynyl, 1-methyl-4-pentynyl, 2-methyl-4-pentynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl or 5-hexynyl, preferably a C3-C4 alkyl group.
“C2-C6 alkynyl group” of “C2-C6 alkynyl group which may be substituted with a group selected from Substituent group α” in the definition of the NR group which may be included in ring A; “C2-C6 alkynyl group” of “C2-C6 alkynyl group which may be substituted with 1 to 5 groups selected from Substituent group α” in the definition of substituent of ring A; “C2-C6 alkynyl group” of “C2-C6 alkynyl group which may be substituted with a group selected from Substituent group β” in the definitions of R1 and R5; and “C2-C6 alkynyl group” in the definitions of R6 and R7 are, for example, ethynyl or the aforementioned “C3-C6 alkynyl group”, preferably a C3-C4 alkynyl group.
“C3-C6 cycloalkyl group” in the definitions of Substituent group δ and Substituent group ε are, for example, cyclopropyl, cyclopentyl or cyclohexyl.
“3- to 7-membered cycloalkyl ring” in the definition of ring A may include an unsaturated bond, and such ring is, for example, cyclopropane, cyclobutane, cyclopentane, cyclopentene, cyclohexane, cyclohexene, cyclohexadiene, cycloheptane or cycloheptadiene.
The aforementioned “3- to 7-membered cycloalkyl ring” may form a fused ring or spiro ring with a 3- to 7-membered heterocyclyl ring or 3- to 7-membered cycloalkyl ring, and such cycloalkyl ring is, for example, 2-oxa-bicyclo[4,3,0]nonan-8-ylidene, 3-oxa-bicyclo[3,3,0]heptan-7-ylidene, 2,4-dioxa-spiro[6.6]undecan-8-ylidene, bicyclo[4,3,0]nonan-7-ylidene, spiro[6.6]undecan-8-ylidene or the like.
In addition, the aforementioned “3- to 7-membered cycloalkyl ring” may not form a fused ring or spiro ring, and may be substituted with an oxo group or a thioxo group.
With respect to the aforementioned “cycloalkyl ring”, a cycloalkyl ring, fused ring which is fused to the cycloalkyl ring, or spiro ring which is spiro bound to the cycloalkyl ring may be substituted with the same or different 1 to 4 (preferably 1 or 2) groups selected from the group consisting of Substituent group α, cyclopropyl C1-C6 alkyl group, C1-C6 alkyl group which may be substituted with 1 to 5 groups selected from Substituent group α, C2-C6 alkenyl group which may be substituted with 1 to 5 groups selected from Substituent group α and C2-C6 alkynyl group which may be substituted with 1 to 5 groups selected from Substituent group α.
Preferred examples of the ring are, 3-hydroxycyclopentane, 4-hydroxycyclohexane, 3-hydroxymethylcyclopentane, 3,4-dihydroxymethylcyclopentane, 4-hydroxymethylcyclohexane, 4,4-dihydroxymethylcyclohexane, 3-(1,2-dihydroxyethyl)cyclopentane, 4-(1,2-dihydroxyethyl)cyclohexane, 3,4-bis(1,2-dihydroxyethyl)cyclopentane, 4,4-bis(1,2-dihydroxyethyl)cyclohexane, 3-(1,2,3-trihydroxypropyl)cyclopentane, 4-(1,2,3-trihydroxypropyl)cyclohexane, 3-(1,2,3,4-tetrahydroxybutyl)cyclopentane, 4-(1,2,3,4-tetrahydroxybutyl)cyclohexane, 3-ethoxycarbonylcyclopentane, 4-ethoxycarbonylcyclohexane, 4,4-diethoxycarbonylcyclchexane, 3-carbamoylcyclopentane, 4-carbamoylcyclohexane, 3-acetylaminocyclopentane, 4-acetylaminocyclohexane, 3,4-diacetylaminomethylcyclopentane, 2,3,4,5-tetrahydroxybicyclo[4,3,0]nonane (the binding position with ring B is the 8-position), 3-oxa-bicyclo[3,3,0]octane (the binding position with ring B is the 7-position), 2,4-dihydroxymethyl-3-oxa-bicyclo[3,3,0]octane (the binding position with ring B is the 7-position), and 2,4-dioxaspiro[5.5]undecane (the binding position with ring B is the 9-position).
“Cycloalkyl ring” in the definition of ring A is, among the aforementioned rings, preferably a 3- to 7-membered cycloalkyl ring which may be substituted with 1 or 2 groups selected from a group consisting of a hydroxy group, hydroxymethyl group, 1,2-dihydroxyethyl group, 1,2,3-trihydroxyethyl group, 1,2,3,4-tetrahydroxybutyl group and acetylamino group, more preferably a 3- to 5-membered saturated cycloalkyl ring which may be substituted with 1 or 2 groups selected from the group consisting of a hydroxymethyl group, 1,2-dihydroxyethyl group, 1,2,3-trihydroxypropyl group, 1,2,3,4-tetrahydroxybutyl group and acetylamino group, and particularly preferably a cyclopropyl or cyclopentyl ring which may be substituted with 1 or 2 groups selected from the group consisting of a hydroxymethyl group, 1,2-dihydroxyethyl group, 1,2,3-trihydroxypropyl group and 1,2,3,4-tetrahydroxybutyl group.
“C3-C10 cycloalkyl group” in the definition of R1 is, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl.
“C4-C12 cycloalkylalkyl group” in the definition of R1 is, for example, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl or cycloheptylmethyl, preferably a C4-C8 cycloalkylalkyl group, more preferably a C4-C7 cycloalkylalkyl group.
With respect to “3- to 7-membered heterocyclyl ring” in the definition of ring A, X and Y included in the ring, independently from each other, represent any one selected from a carbon atom, a group having the formula NR (R represents a hydrogen atom or a C1-C6 alkyl, C2-C6 alkenyl, C2-C6 group or C1-C6 alkylcarbonyl group which may be substituted with a group selected from Substituent group α), an oxygen atom, a sulfur atom, a group having the formula SO and a group having the formula SO2, preferably any one selected from a carbon atom, an oxygen atom, a sulfur atom, a group having the formula SO, and a group having the formula SO2. The 3- to 7-membered heterocyclyl ring may include an unsaturated bond.
Examples of such ring are, a heterocyclyl ring including a nitrogen atom such as aziridine, azetidine, pyrrolidine, pyrroline, piperidine and imidazolidine; a heterocyclyl ring including an oxygen atom such as oxirane, oxetane, tetrahydrofuran, oxolene, tetrahydropyran, dihydropyran, oxepane, 1,3-dioxclane, 1,3-dioxane and 1,3-dioxepane; a heterocyclyl ring including a sulfur atom, a group having the formula SO or a group having the formula SO2 such as thiirane, thietane, thiolane, thiolene, thiane, thiepane, 1,3-dithiolane, 1,3-dithiane, 1,3-dithiepane, 1,3-dioxo-1,3-dithiolane, 1,3-dioxo-1,3-dithiane, 1,1,3,3-tetraoxo-1,3-dithiolane and 1,1,3,3-tetraoxo-1,3-dithiane; a heterocyclyl ring including an oxygen atom and a sulfur atom such as 1,3-oxathiolane, 1,3-oxathiane and 1,3-oxathiepane; a heterocyclyl ring including a nitrogen atom and an oxygen atom such as 1,3-oxapyrrolidine and 1,3-oxapyrroline; and a heterocyclyl ring including a nitrogen atom and a sulfur atom such as 1,3-thiapyrrolidine and 1,3-thiapyrroline.
Preferably, it is oxirane, tetrahydrofuran, tetrahydropyran, 1,3-dioxolane, 1,3-dioxane, 1,3-dioxepane, 1,3-dithiolane, 1,3-dithiane, 1,1,3,3-tetraoxo-1,3-dithiolane, 1,3-oxathiolane, 1,3-oxathiane or 1,3-oxathiepane.
More preferably, it is oxirane, tetrahydrofuran, 1,3-dioxolane, 1,3-dioxane, 1,3-dithiolane, 1,3-dithiane, 1,3-oxathiolane or 1,3-oxathiane.
Even more preferably, it is oxirane, 1,3-dioxolane, 1,3-dioxane or 1,3-oxathiolane.
The aforementioned “3- to 7-membered heterocyclyl ring” may form a fused ring or spiro ring with a 3- to 7-membered heterocyclyl ring or 3- to 7-membered cycloalkyl ring, preferably may form a fused ring or spiro ring with a 5- or 6-membered heterocyclyl ring (the heterocyclyl ring includes 1 or 2 oxygen and/or nitrogen atoms as hetero atom) or 5- or 6-membered cycloalkyl ring, and more preferably may form a fused ring or spiro ring with tetrahydrofuran, tetrahydropyran, pyrrolidine, piperidine, 1,3-dioxane or cyclohexyl ring.
Examples of such heterocyclyl ring are 2,4-dioxa-bicyclo[3,3,0]octane (the binding position with ring B is the 3-position), 2,4,7-trioxa-bicyclo[3,3,0]octane (the binding position with ring B is the 3-position), 7,9-dioxa-bicyclo[4,3,0]nonane (the binding position with ring B is the 8-position), 7-aza-2,4-dioxa-bicyclo[3,3,0]octane (the binding position with ring B is the 3-position), 2,4,8,10-tetraoxaspiro[5,5]undecane (the binding position with ring B is the 3-position) and the like. The binding position of these rings with ring B is the same as the aforedescribed one.
In addition, the aforementioned “3- to 7-membered heterocyclyl ring” may not form a fused ring or spiro ring, and may be substituted with an oxo group or a thioxo group.
With respect to the aforementioned “heterocyclyl ring”, heterocyclyl ring, fused ring which is fused to the heterocyclyl ring or spiro ring which is spiro bound to the heterocyclyl ring may be substituted with the same or different 1 to 4 (preferably 1 or 2) substituents.
The substituent is a group selected from the group consisting of an oxo group, a thioxo group, Substituent group α, a cyclopropyl C1-C6 alkyl group, a C1-C6 alkyl group which may be substituted with 1 to 5 groups selected from Substituent group α, a C2-C6 alkenyl group which may be substituted with 1 to 5 groups selected from Substituent group α and a C2-C6 alkynyl group which may be substituted with 1 to 5 groups selected from Substituent group α.
The substituent is preferably a group selected from the group consisting of an oxo group, a thioxo group, Substituent group α, a cyclopropyl C1-C6 alkyl group and a C1-C6 alkyl group which may be substituted with 1 to 5 groups selected from Substituent group α.
More preferably, it is a group selected from the group consisting of an oxo group, a thioxo group, Substituent group α and a C1-C6 alkyl group which may be substituted with 1 to 4 groups selected from Substituent group α.
Even more preferably, it is 1 or 2 groups selected from the group consisting of an oxo group, a thioxo group, Substituent group α(Substituent group α is a hydroxy group and a group having the formula NR6R7, and R6 and R7, independently from each other, represent a hydrogen atom or C1-C6 alkylcarbonyl group), a methyl group, an ethyl group and a C1-C6 alkyl group substituted with 1 to 4 hydroxy groups.
Further preferably, it is 1 or 2 groups selected from the group consisting of Substituent group α [Substituent group α represents a hydroxy group and a group having the formula NR6R7 (R6 and R7, independently from each other, represent a hydrogen atom or methylcarbonyl group)], a methyl group, an ethyl group, a hydroxymethyl group, a 1,2-dihydroxyethyl group, a 1,2,3-trihydroxypropyl group and a 1,2,3,4-tetrahydroxybutyl group.
As for such examples,
“C6-C10 aryl group” of “C6-C10 aryl group which may be substituted with a group selected from Substituent group β” in the definition of Substituent group γ; and “C6-C10 aryl group” in the definitions of Substituent group δ and Substituent group ε are, for example, phenyl or naphthyl.
With respect to the “C6-C10 aryl group which may be substituted with a group selected from Substituent group β”, the “C6-C10 aryl group” is substituted with a substituent selected from Substituent group β at a substitutable position, the substituent is not limited to one, and may be the same or different plural (2 to 4) substituents.
“5- or 6-membered heteroaryl group” in the definition of R3 includes 1 to 3 hetero atoms selected from a nitrogen atom, an oxygen atom and a sulfur atom. As for such heteroaryl, for example, furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyridyl, piridazinyl, pyrimidinyl and pyradinyl can be mentioned, and it is preferably furyl, thienyl, pyrrolyl, pyridyl or pyrimidinyl, more preferably pyrrolyl.
“5-membered heteroaryl group” in the definitions of Substituent group δ and Substituent group ε is, for example, 1,2,3-triazolyl, 1,2,4-triazolyl, tetrazolyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, thiadiazolyl, thienyl or furyl.
“Halogeno C1-C6 alkyl group” in the definition of Substituent group δ is, for example, trifluoromethyl or trifluoroethyl.
“Halogeno C1-C14 alkyl group” in the definition of Substituent group ε is, for example, the aforementioned “halogeno C1-C6 alkyl group”, 4,4,4-trifluorobutyl, 5,5,5-trifluoropentyl, 6,6,6-trifluorohexyl, 7,7,7-trifluoroheptyl or 8,8,8-trifluorooctyl, preferably a halogeno C4-C8 alkyl group.
“C1-C6 alkoxy group” in the definitions of Substituent group α, Substituent group β and Substituent group δ represents a group in which an oxygen atom is bound to the aforementioned “C1-C6 alkyl group”, for example, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, s-butoxy, t-butoxy, pentoxy, isopentoxy, 2-methylbutoxy, 1-ethylpropoxy, 2-ethylpropoxy, neopentoxy, hexyloxy, 4-methylpentoxy, 3-methylpentoxy, 2-methylpentoxy, 3,3-dimethylbutoxy, 2,2-dimethylbutoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy or 2,3-dimethylbutoxy, preferably a C1-C4 alkoxy group, and more preferably C1-C2 alkoxy group.
“C1-C14 alkoxy group” in the definition of Substituent group ε represents a group in which an oxygen atom is bound to the aforementioned “C1-C14 alkyl group”, for example, the aforementioned “C1-C6 alkoxy group”, octyloxy, nonyloxy, decyloxy, dodecyloxy, tetradecyloxy or the like, preferably a C1-C10 alkoxy group, and more preferably a C4-C8 alkoxy group.
“Halogeno C1-C6 alkoxy group” in the definitions of Substituent group α and Substituent group δ represents a group in which one or two or more hydrogen atoms of the aforementioned “C1-C6 alkyl group” are substituted with the aforementioned “halogen atom”. Preferably, it is a halogeno C1-C4 alkoxy group, more preferably difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethoxy, and even more preferably trifluoromethoxy.
“Halogeno C1-C14 alkoxy group” in the definition of Substituent group ε represents a group in which one or two or more hydrogen atoms of the aforementioned “C1-C14 alkyl group” are substituted with the aforementioned “halogen atom”. Preferably, it is a halogeno C1-C10 alkoxy group, more preferably a halogeno C4-C8 alkoxy group, and even more preferably 4,4,4-trifluorobutoxy, 5,5,5-trifluoropentyloxy, 6,6,6-trifluorohexyloxy, 7,7,7-trifluoroheptyloxy or 8,8,8-trifluorooctyloxy.
“C3-C10 cycloalkyloxy group” in the definition of Substituent group γ is, for example, cyclopropyloxy, cyclohexyloxy or the like.
“C6-C10 aryloxy group” in the definition of Substituent group γ is, for example, phenoxy or naphthyloxy.
“C7-C19 aralkyloxy group” in the definition of Substituent group γ is, for example, benzyloxy, 1-phenylethyloxy, 2-phenylethyloxy, benzhydryloxy or 1-naphthylmethyloxy.
“C1-C6 alkylthio group” in the definitions of Substituent group β and Substituent group δ represents a group in which a sulfur atom is bound to the aforementioned “C1-C6 alkyl group”, and the sulfur atom may be oxidized. Preferably, it is a C1-C4 alkylthio group, for example, methylthio, ethylthio, n-propylthio, n-butylthio, methylsulfinyl or methylsulfonyl.
With respect to “C1-C14 alkylthio group” in the definition of Substituent group ε, the sulfur atom to which the alkyl group is bound may be oxidized, and it is for example, the aforementioned “C1-C6 alkylthio group”, n-heptylthio, 3-methylhexylthio, n-octylthio, 2,4-dimethylhexylthio, n-octylthio, or 2,3,6-trimethylheptylthio, preferably a C1-C10 alkylthio group, and more preferably a C4-C8 alkylthio group.
With respect to “C3-C10 cycloalkylthio group” in the definition of Substituent group γ, the sulfur atom may be oxidized, and it is for example, cyclopropylthio, cyclohexylthio, cyclopentylsulfinyl or cyclohexylsulfonyl.
With respect to “C6-C10 arylthio group” in the definition of Substituent group γ, the sulfur atom may be oxidized, and it is for example, phenylthio, naphthylthio, phenylsulfinyl or phenylsulfonyl.
With respect to “C7-C19 aralkylthio group” in the definition of Substituent group γ, the sulfur atom may be oxidized, and it is for example, benzylthio, phenylethylthio, benzhydrylthio, benzylsulfinyl or benzylsulfonyl.
“C1-C6 alkanoyl group” in the definitions of R6, R7, Substituent group β and Substituent group δ represents a group in which a hydrogen atom or C1-C5 alkyl group is bound to a carbonyl group, and is for example, formyl, acetyl, propionyl, butyryl, valeryl or pyvaloyl.
“C1-C14 alkanoyl group” in the definition of Substituent group ε is, for example, the aforementioned “C1-C6 alkanoyl group”, octanoyl, decanoyl, dodecanoyl or tetradecanoyl.
“C2-C4 alkenyl-carbonyl group” in the definition of Substituent group β is, for example, acryloyl or crotonoyl.
“C2-C6 alkenyl-carbonyl group” in the definitions of R6 and R7 is, for example, the aforementioned “C2-C4 alkenyl-carbonyl group”, 1,3-butadienylcarbonyl or 3-methyl-2-butenylcarbonyl.
“C6-C10 aryl-carbonyl group” in the definition of Substituent group γ is, for example, benzoyl, naphthoyl or phenylacetyl.
“C1-C6 alkoxy-carbonyl group” in the definitions of Substituent group α and Substituent group δ represents a group in which the aforementioned “C1-C6 alkoxy group” is bound to a carbonyl group, and is for example, methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, tert-butoxycarbonyl or the like.
“C1-C10 alkoxy-carbonyl group” in the definition of Substituent group β is, for example, the aforementioned “C1-C6 alkoxycarbonyl group”, heptyloxy, octyloxy, nonyloxy or decyloxy.
“C1-C14 alkoxy-carbonyl group” in the definition of Substituent group ε is, for example, the aforementioned “C1-C10 alkoxy-carbonyl group”, dodecyloxycarbonyl or tetradecyloxycarbonyl, preferably a C1-C10 alkoxy-carbonyl group, and more preferably a C4-C8 alkoxy-carbonyl group.
“C3-C6 cycloalkyloxycarbonyl group” in the definition of Substituent group γ is, for example, cyclopropyloxycarbonyl, cyclopentyloxycarbonyl, cyclohexyloxycarbonyl or norbornyloxycarbonyl.
“C6-C10 aryloxy-carbonyl group” in the definition of Substituent group γ is, for example, phenoxycarbonyl or naphthyloxycarbonyl.
“C7-C19 aralkyloxy-carbonyl group” in the definition of Substituent group γ is, for example, benzyloxycarbonyl, benzhydryloxycarbonyl or 2-phenethyloxycarbonyl.
“C2-C6 alkanoyloxy group” in the definition of Substituent group β represents a group in which the C2-C6 alkanoyl group is bound to an oxygen atom, and is for example, acetoxy, propionyloxy, butyryloxy, valeryloxy or pivaloyloxy.
“C1-C10 alkoxy-carbonyloxy group” in the definition of Substituent group β is, for example, methoxycarbonyloxy, ethoxycarbonyloxy, n-propoxycarbonyloxy, isopropoxycarbonyloxy, n-butoxycarbonyloxy, tert-butoxycarbonyloxy, n-pentyloxycarbonyloxy or n-hexyloxycarbonyloxy.
“C6-C10 aryl-carbonyloxy group” in the definition of Substituent group γ is, for example, benzoyloxy, naphthyloxy or phenylacetoxy.
“Carbamoyl group which may be substituted with a group selected from a C1-C6 alkyl group, C2-C6 alkenyl group, C2-C6 alkynyl group, C1-C6 alkanoyl group or C2-C6 alkenyl-carbonyl group” in the definition of Substituent group α is a carbamoyl group or cyclic aminocarbonyl group which may be substituted with 1 or 2 substituents selected from C1-C6 alkyl groups such as methyl, ethyl, propyl and the like, C2-C6 alkenyl groups such as vinyl, allyl, isopropenyl and the like, C2-C6 alkynyl groups such as ethynyl and the like, C1-C6 alkanoyl groups such as acetyl and the like, and C2-C6 alkenyl-carbonyl groups such as acryloyl and the like, preferably, specifically for example, a carbamoyl group or cyclic aminocarbonyl group which may be substituted with 1 or 2 substituents selected from a C1-C6 alkyl group and a C1-C6 alkanoyl group, more preferably a carbamoyl group or cyclic aminocarbonyl group which is substituted with 1 or 2 C1-C2 alkanoyl groups. Specifically, it is carbamoyl, N-methylcarbamoyl, N-ethylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl or N-acetylcarbamoyl, preferably N-acetyl carbamoyl.
“Carbamoyl group which may be substituted with a group selected from a C1-C4 alkyl group, phenyl group, C1-C7 acyl group and C1-C4 alkoxyphenyl group” in the definition of Substituent group β is a carbamoyl group or cyclic aminocarbonyl group which may be substituted with 1 or 2 substituents selected from C1-C4 alkyl groups such as methyl, ethyl and the like, phenyl group, C1-C7 acyl groups such as acetyl, propionyl, benzoyl and the like, and C1-C4 alkoxyphenyl groups such as methoxyphenyl and the like, specifically for example, carbamoyl, N-methylcarbamoyl, N-ethylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl, N-phenylcarbamoyl, N-acetylcarbamoyl, N-benzoylcarbamoyl, N-(p-methoxyphenyl)carbamoyl, 1-pyrrolidinylcarbonyl, piperidinocarbonyl, 1-piperadinylcarbonyl or morpholinocarbonyl.
“Thiocarbamoyl group which may be substituted with a C1-C4 alkyl group or phenyl group” in the definition of Substituent group β is a thiocarbamoyl group which may be substituted with 1 or 2 substituents selected from C1-C4 alkyl groups such as methyl, ethyl and the like, and a phenyl group, specifically for example, thiocarbamoyl, N-methylthiocarbamoyl or N-phenylthiocarbamoyl.
“Carbamoyloxy group which may be substituted with a C1-C4 alkyl group or phenyl group” in the definition of Substituent group β is a carbamoyloxy group which may be substituted with 1 or 2 substituents selected from C1-C4 alkyl groups such as methyl, ethyl and the like, and a phenyl group, specifically for example, carbamoyloxy, N-methyl carbamoyloxy, N,N-dimethyl carbamoyloxy, N-ethylcarbamoyloxy or N-phenyl carbamoyloxy.
With respect to “group having the formula NR6R7” in the definitions of Substituent group α, Substituent group δ and Substituent group ε, R6 and R7, independently from each other, represent a hydrogen atom, C1-C6 alkyl group, C2-C6 alkenyl group, C2-C6 alkynyl group, C1-C6 alkanoyl group or C2-C6 alkenyl-carbonyl group, or, together with the nitrogen atom to which R6 and R7 are bound, form a heterocyclyl group. Preferably, it is a group in which R6 and R7 are a hydrogen atom, C1-C6 alkyl group or C1-C6 alkanoyl group, more preferably a group in which R6 and R7 are a hydrogen atom, C1-C4 alkyl group or C1-C4 alkanoyl group, even more preferably a group in which R6 and R7 are a hydrogen atom or C1-C2 alkanoyl group. Specifically it is amino, methylamino, ethylamino, dimethylamino, diethylamino or acetylamino, preferably acetylamino.
“C1-C6 alkanoylamino group” in the definitions of Substituent group β and Substituent group δ is, for example, acetamide, propionamide, butyramide, valeroamide or pivaloamide.
“C1-C14 alkanoylamino group” in the definition of Substituent group ε is, for example, the aforementioned “C1-C6 alkanoylamino group”, octanoylamino, decanoylamino, dodecanoylamino or tetradecanoylamino.
“C1-C10 alkoxy-carboxamide group” in the definition of Substituent group β is, for example, methoxycarboxamide, ethoxycarboxamide or tert-butoxycarboxamide.
“Ureido group which may be substituted with a C1-C4 alkyl group or phenyl group” in the definition of Substituent group β is, for example, an ureido group which may be substituted with 1 to 3 (preferably 1 or 2) substituents selected from C1-C4 alkyl groups such as a methyl group, ethyl group and the like, and a phenyl group, and it is for example, ureido, 1-methylureido, 3-methylureido, 3,3-dimethylureido, 1,3-dimethylureido or 3-phenylureido.
“C6-C10 aryl-carbonylamino group” in the definition of Substituent group γ is, for example, benzamide, naphthoamide or phthalimide.
“C6-C10 aryloxy-carboxamide group” in the definition of Substituent group γ is, for example, phenoxycarboxamide.
“C7-C19 aralkyloxy-carboxamide group” in the definition of Substituent group γ is, for example, benzyloxycarboxamide or benzhydryloxycarboxamide.
“C3-C10 cycloalkyloxy-carbonyloxy group” in the definition of Substituent group γ is, for example, cyclopropyloxycarbonyloxy or cyclohexyloxycarbonyloxy.
“C6-C10 aryloxy-carbonyloxy group” in the definition of Substituent group γ is, for example, phenoxycarbonyloxy or naphthyloxycarbonyloxy.
“C7-C19 aralkyloxy-carbonyloxy group” in the definition of Substituent group γ is, for example, benzyloxycarbonyloxy, 1-phenylethyloxycarbonyloxy, 2-phenylethyloxycarbonyloxy or benzhydryloxycarbonyloxy.
“Heterocyclyl group” in the definition of Substituent group γ; and “heterocyclyl group” of “heterocyclyloxy group”, “heterocyclylthio group”, “heterocyclylsulfinyl group”, “heterocyclylsulfonyl group” and “heterocyclyloxycarbonyl group” represent a 5- to 8-membered ring (preferably 5- or 6-membered ring) group or a fused ring group thereof, which contains 1 to several (preferably 1 to 4) hetero atoms such as nitrogen atoms (may be oxidized), oxygen atoms and sulfur atoms. Examples of such “heterocyclyl group” are pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, tetrazolyl, furyl, thienyl, oxazolyl, isoxazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, thiazolyl, isothiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, indolyl, pyranyl, thiopyranyl, dioxynyl, dioxolyl, quinolyl, pyrido[2,3-d]pyrimidyl, 1,5-, 1,6-, 1,7-, 1,8-, 2,6- or 2,7-naphthylidyl group, thieno[2,3-d]pyridyl, benzopyranyl, tetrahydrofuryl, tetrahydropyranyl, dioxolanyl and dioxanyl.
These heterocyclyl groups may be substituted at substitutable positions with 1 to 3 substituents selected from C1-C4 alkyl groups such as methyl, ethyl and the like, a hydroxy group, an oxo group and C1-C4 alkoxy groups such as methoxy, ethoxy and the like.
“C1-C6 alkyl-carbamoyl group” in the definition of Substituent group δ is, for example, methylcarbamoyl, dimethylcarbamoyl or propylcarbamoyl.
“C1-C14 alkyl-carbamoyl group” in the definition of Substituent group ε is, for example, the aforementioned “C1-C6 alkyl-carbamoyl group”, octylcarbamoyl, decylcarbamoyl, dodecylcarbamoyl or tetradecylcarbamoyl, preferably a C1-C10 alkyl-carbamoyl group, and more preferably a C4-C8 alkyl-carbamoyl group.
“C1-C6 alkoxy-carbonyl C1-C6 alkyl-carbamoyl group” in the definition of Substituent group δ is, for example, butoxycarbonylmethylcarbamoyl or ethoxycarbonylmethylcarbamoyl.
“C1-C14 alkoxy-carbonyl C1-C14 alkyl-carbamoyl group” in the definition of Substituent group ε is, for example, the aforementioned “C1-C6 alkoxy-carbonyl C1-C6 alkyl-carbamoyl group” or octyloxycarbonylmethylcarbamoyl, preferably a C1-C10 alkoxy-carbonyl C1-C10 alkyl-carbamoyl group, and more preferably a C4-C8 alkoxy-carbonyl C4-C8 alkyl-carbamoyl group.
“1,3-diacylguanidino C1-C6 alkyl group” in the definition of Substituent group δ is, for example, 1,3-diacetylguanidinomethyl or 1,3-bis-tert-butoxycarbonylguanidinomethyl.
“1,3-diacylguanidino C1-C14 alkyl group” in the definition of Substituent group ε is, for example, the aforementioned “1,3-diacylguanidino C1-C6 alkyl group”, 1,3-diacetylguanidinooctyl or 1,3-bis-tert-butoxycarbonylguanidinooctyl, preferably a 1,3-diacylguanidino C1-C10 alkyl group, and more preferably a 1,3-diacylguanidino C4-C8 alkyl group.
X and Y represent a group in which X and Y together with the carbon atom of ring B to which they are bound form ring A, respectively represent a hydrogen atom, or X and Y together represent a substituent of ring B (the substituent is an oxo group or a thioxo group), and preferably represent a group in which X and Y together with the carbon atom of ring B to which they are bound form ring A, or respectively represent a hydrogen atom.
In a preferred example, in the case where X and Y represent a group in which X and Y together with the carbon atom of ring B to which they are bound form ring A, ring A is a 3- to 7-membered heterocyclyl ring or 3- to 7-membered saturated cycloalkyl ring.
With respect to the heterocyclyl ring, X and Y included in the ring, independently from each other, represent any one selected from a carbon atom, a group having the formula NR (R represents a hydrogen atom, a C1-C6 alkyl group which may be substituted with a group selected from Substituent group α, a C2-C6 alkenyl group which may be substituted with a group selected from Substituent group α, a C2-C6 alkynyl group which may be substituted with a group selected from Substituent group α or a C1-C6 alkanoyl group which may be substituted with a group selected from Substituent group α), an oxygen atom, a sulfur atom, a group having the formula SO and a group having the formula SO2,
The 3- to 7-membered saturated cycloalkyl ring may be substituted with 1 or 2 groups selected from the group consisting of a hydroxy group, a hydroxymethyl group, a 1,2-dihydroxyethyl group, a 1,2,3-trihydroxypropyl group, a 1,2,3,4-tetrahydroxybutyl group and an acetylamino group.
Ring A is, more preferably, a 3- to 7-membered heterocyclyl ring or 3- to 5-membered cycloalkyl ring.
With respect to the heterocyclyl ring which is a more preferred example of ring A, X and Y included in the ring, independently from each other, represent any one selected from a carbon atom, an oxygen atom, a sulfur atom, a group having the formula SO and a group having the formula SO2,
The 3- to 5-membered cycloalkyl ring may be substituted with 1 or 2 groups selected from the group consisting of a hydroxymethyl group, a 1,2-dihydroxyethyl group, a 1,2,3-trihydroxypropyl group, a 1,2,3,4-tetrahydroxybutyl group and an acetylamino group.
Ring A is, more preferably, the heterocyclyl ring or the undermentioned cyclopropyl or cyclopentyl ring described below.
Examples of such heterocyclyl ring are,
In addition, the cyclopropyl or cyclopentyl ring is a cyclopropyl or cyclopentyl ring which may be substituted with 1 or 2 groups selected from the group consisting of a hydroxymethyl group, a 1,2-dihydroxyethyl group, a 1,2,3-trihydroxypropyl group and a 1,2,3,4-tetrahydroxybutyl group.
Ring A is, further preferably for example,
Ring A is, particularly preferably,
Preferred specific examples of ring A are,
Ring B is a 5- to 7-membered cycloalkene group. Here, l and m, which are parameters to determine the number of members of ring B, independently from each other, are an integer of 0 to 3, and l+m is 1 to 3. The l+m being 1 to 3 represents that ring B is 5- to 7-membered. Preferably, 1 is 0, and m is an integer of 1 to 3. More preferably, it is a cyclohexynyl group in which l is 0, and m is 1.
Among the groups defined as R1, preferred is a hydroxy group, halogen atom, C1-C6 alkyl group or C1-C6 alkoxy group, more preferred is a hydroxy group, fluorine atom, chlorine atom, methyl group, ethyl group, propyl group, methoxy group or ethoxy group, further preferred is a fluorine atom or methyl group.
The number of substitutions n, which is the number of R1 that are substituted to ring B, is 0 to 3, preferably 0 or 1. More preferably, n is 0.
Among the groups defined as R2, preferred is a C1-C6 alkyl group which may be substituted with a group selected from Substituent group β, more preferred is a C1-C6 alkyl group, further preferred is a C1-C4 alkyl group, and particularly preferred is an ethyl group.
Among the groups defined as R3, “5- or 6-membered heteroaryl group” of “5- or 6-membered heteroaryl group which may be substituted with a group selected from Substituent group ε” is particularly preferably a pyrrolyl group. That is, preferably R3 is a phenyl or pyrrolyl group which may be substituted with a group selected from Substituent group ε. Preferably, it is a phenyl or pyrrolyl group which may be substituted with a group selected from a halogen atom, C1-C14 alkyl group and halogeno C1-C14 alkyl group, more preferably a phenyl or pyrrolyl group which may be substituted with a group selected from a fluorine atom, chlorine atom, C1-C10 alkyl group, halogeno C1-C10 alkyl group and cyclopropyl C1-C10 alkyl group, even more preferably a phenyl or pyrrolyl group which may be substituted with a group selected from a fluorine atom, chlorine atom, bromine atom, C3-C8 alkyl group and halogeno C4-C8 alkyl group, and further preferably a phenyl group which may be substituted with a group selected from a fluorine atom, chlorine atom and C3-C8 alkyl group.
In addition, in the case where it is substituted by a substituent, the position of substitution is preferably the 2-position or 4-position.
R3 is, for example,
Among them, specific examples are preferably,
With respect to the “pharmacologically acceptable salts thereof”, since the compound having the general formula (I) of the present invention can be converted to a salt by reaction with an acid in the case where it has a basic group such as an amino group, or by reaction with a base in the case where it has an acidic group such as a carboxyl group, salts thereof are represented.
Salts of a basic group are preferably inorganic acid salts such as hydrohalogenic acid salts including hydrochloride, hydrobromide and hydroiodide, nitrates, perchlorates, sulfates, phosphates or the like; lower alkanesulfonic acid salts such as methanesulfonate, trifluoromethanesulfonate and ethanesulfonate, arylsulfonic acid salts such as benzene sulfonate and p-toluenesulfonate, organic acid salts such as acetate, malates, fumarates, succinates, citrates, ascorbates, tartrates, oxalates, maleates or the like; and amino acid salts such as glycine salt, lysine salt, arginine salt, ornithine salt, glutamate and aspartate,
On the other hand, salts of an acidic group are preferably alkali metal salts such as sodium salt, potassium salt and lithium salt, alkaline earth metal salts such as calcium salt and magnesium salt, metal salts such as aluminum salt and iron salt; inorganic salts such as ammonium salt, amine salts including organic salts such as t-octylamine salt, dibenzylamine salt, morpholine salt, glucosamine salt, phenylglycine alkyl ester salt, ethylenediamine salt, N-methylglucamine salt, guanidine salt, diethylamine salt, triethylamine salt, dicyclohexylamine salt, N,N′-dibenzylethylenediamine salt, chloroprocaine salt, procaine salt, diethanolamine salt, N-benzylphenethylamine salt, piperazine salt, tetramethylammonium salt and tris(hydroxymethyl)aminomethane salt; and amino acid salts such as glycine salt, lysine salt, arginine salt, ornithine salt, glutamate and aspartate.
The compounds having the general formula (I) according to the present invention or pharmacologically acceptable salts thereof have an asymmetric carbon atom in their molecules, and thus stereoisomers of R configuration and S configuration exist. Each of them, or a compound with an arbitrary ratio of these, is also included in the present invention. With respect to such stereoisomers, the compound (I) can be synthesized by using an optically resolved starting compound, or a synthesized compound (I) can be optically resolved by ordinary optical resolution or separation methods if desired.
There exist optical isomers with respect to the compound having the general formula (I) according to the present invention or pharmacologically acceptable salts thereof, and each of the optical isomers and mixtures of such isomers are also included in the present invention.
When the compound having the general formula (I) and pharmacologically acceptable salts thereof are exposed to the atmosphere or are recrystallized, they may absorb moisture, resulting in cases such as the adhesion of adsorbed water and the generation of hydrates. Such hydrated compounds and salts are also included in the present invention.
As representative compounds of the present invention, the compounds listed in the following Tables 1 to 3 can be mentioned for example, but the present invention is not limited to these compounds.
Abbreviations and “ring 1” to “ring 21” in the tables are as follows.
In the Tables, “di” indicates that there are two identical substituents, and “tri” indicates that there are three identical substituents.
##STR00003## ##STR00004## ##STR00005##
The binding position of rings 1 to 21 with ring B is the position indicated by a black dot, which is located at the right end of the aforementioned chemical structure.
The substituents represented by the abbreviations as X and Y in Table 1, are shown below.
##STR00006## ##STR00007## ##STR00008##
TABLE 1
##STR00009##
Compound
No.
X, Y
R3
1-1
O═
Ph
1-2
S═
Ph
1-3
cPr
Ph
1-4
cBu
Ph
1-5
cPent
Ph
1-6
cHex
Ph
1-7
cHept
Ph
1-8
oxi
Ph
1-9
oxe
Ph
1-10
oxo
Ph
1-11
oxa
Ph
1-12
dioxo
Ph
1-13
dioxa
Ph
1-14
dioxe
Ph
1-15
dithio
Ph
1-16
dithia
Ph
1-17
ring 1
Ph
1-18
ring 2
Ph
1-19
oxathio
Ph
1-20
oxathia
Ph
1-21
ozl
Ph
1-22
ozn
Ph
1-23
tzl
Ph
1-24
tzn
Ph
1-25
3-HM-cPent
Ph
1-26
4-HM-dioxo
Ph
1-27
4-HM-dithio
Ph
1-28
4-HM-oxathio
Ph
1-29
3,4-diHM-cPent
Ph
1-30
4,5-diHM-dioxo
Ph
1-31
4,5-diHM-dithio
Ph
1-32
4,5-diHM-oxathio
Ph
1-33
3,4-diHE-cPent
Ph
1-34
4,5-diHE-dioxo
Ph
1-35
4,5-diHE-dithio
Ph
1-36
4,5-diHE-oxathio
Ph
1-37
3-HE-cPent
Ph
1-38
4-HE-dioxo
Ph
1-39
4-HE-dithio
Ph
1-40
4-HE-oxathio
Ph
1-41
3-HP-cPent
Ph
1-42
4-HP-dioxo
Ph
1-43
4-HP-dithio
Ph
1-44
4-HP-oxathio
Ph
1-45
3-HB-cPent
Ph
1-46
4-HB-dioxo
Ph
1-47
4-HB-dithio
Ph
1-48
4-HB-oxathio
Ph
1-49
ring 3
Ph
1-50
ring 4
Ph
1-51
ring 5
Ph
1-52
ring 6
Ph
1-53
ring 7
Ph
1-54
ring 8
Ph
1-55
ring 9
Ph
1-56
ring 10
Ph
1-57
3,4-diCH2NHAc-cPent
Ph
1-58
4,5-diCH2NHAc-dioxo
Ph
1-59
4,5-diCH2NHAc-dithio
Ph
1-60
4,5-diCH2NHAc-oxathio
Ph
1-61
ring 11
Ph
1-62
ring 12
Ph
1-63
ring 13
Ph
1-64
ring 14
Ph
1-65
4-OH-cHex
Ph
1-66
5-OH-dioxa
Ph
1-67
5-OH-dithia
Ph
1-68
5-OH-oxathia
Ph
1-69
4-NHAc-cHex
Ph
1-70
5-NHAc-dioxa
Ph
1-71
5-NHAc-dithia
Ph
1-72
5-NHAc-oxathia
Ph
1-73
4,4-diMe-cHex
Ph
1-74
5,5-diMe-dioxa
Ph
1-75
5,5-diMe-dithia
Ph
1-76
5,5-diMe-oxathia
Ph
1-77
4,4-diHM-cHex
Ph
1-78
5,5-diHM-dioxa
Ph
1-79
5,5-diHM-dithia
Ph
1-80
5,5-diHM-oxathia
Ph
1-81
ring 15
Ph
1-82
ring 16
Ph
1-83
ring 17
Ph
1-84
ring 18
Ph
1-85
4,4-diCO2Et-cHex
Ph
1-86
5,5-diCO2Et-dioxa
Ph
1-87
5,5-diCO2Et-dithia
Ph
1-88
5,5-diCO2Et-oxathia
h
1-89
O═
4-F—Ph
1-90
S═
4-F—Ph
1-91
cPr
4-F—Ph
1-92
cBu
4-F—Ph
1-93
cPent
4-F—Ph
1-94
cHex
4-F—Ph
1-95
cHept
4-F—Ph
1-96
oxi
4-F—Ph
1-97
oxe
4-F—Ph
1-98
oxo
4-F—Ph
1-99
oxa
4-F—Ph
1-100
dioxo
4-F—Ph
1-101
dioxa
4-F—Ph
1-102
dioxe
4-F—Ph
1-103
dithio
4-F—Ph
1-104
dithia
4-F—Ph
1-105
ring 1
4-F—Ph
1-106
ring 2
4-F—Ph
1-107
oxathio
4-F—Ph
1-108
oxathia
4-F—Ph
1-109
ozl
4-F—Ph
1-110
ozn
4-F—Ph
1-111
tzl
4-F—Ph
1-112
tzn
4-F—Ph
1-113
3-HM-cPent
4-F—Ph
1-114
4-HM-dioxo
4-F—Ph
1-115
4-HM-dithio
4-F—Ph
1-116
4-HM-oxathio
4-F—Ph
1-117
3,4-diHM-cPent
4-F—Ph
1-118
4,5-diHM-dioxo
4-F—Ph
1-119
4,5-diHM-dithio
4-F—Ph
1-120
4,5-diHM-oxathio
4-F—Ph
1-121
3,4-diHE-cPent
4-F—Ph
1-122
4,5-diHE-diaxo
4-F—Ph
1-123
4,5-diHE-dithio
4-F—Ph
1-124
4,5-diHE-oxathio
4-F—Ph
1-125
3-HE-cPent
4-F—Ph
1-126
4-HE-dioxo
4-F—Ph
1-127
4-HE-dithio
4-F—Ph
1-128
4-HE-oxathio
4-F—Ph
1-129
3-HP-cPent
4-F—Ph
1-130
4-HP-dioxo
4-F—Ph
1-131
4-HP-dithio
4-F—Ph
1-132
4-HP-oxathio
4-F—Ph
1-133
3-HB-cPent
4-F—Ph
1-134
4-HB-dioxo
4-F—Ph
1-135
4-HB-dithio
4-F—Ph
1-136
4-HB-oxathio
4-F—Ph
1-137
ring 3
4-F—Ph
1-138
ring 4
4-F—Ph
1-139
ring 5
4-F—Ph
1-140
ring 6
4-F—Ph
1-141
ring 7
4-F—Ph
1-142
ring 8
4-F—Ph
1-143
ring 9
4-F—Ph
1-144
ring 10
4-F—Ph
1-145
3,4-diCH2NHAc-cPent
4-F—Ph
1-146
4,5-diCH2NHAc-dioxo
4-F—Ph
1-147
4,5-diCH2NHAc-dithio
4-F—Ph
1-148
4,5-diCH2NHAc-oxathio
4-F—Ph
1-149
ring 11
4-F—Ph
1-150
ring 12
4-F—Ph
1-151
ring 13
4-F—Ph
1-152
ring 14
4-F—Ph
1-153
4-OH-cHex
4-F—Ph
1-154
5-OH-dioxa
4-F—Ph
1-155
5-OH-dithia
4-F—Ph
1-156
5-OH-oxathia
4-F—Ph
1-157
4-NHAc-cHex
4-F—Ph
1-158
5-NHAc-dioxa
4-F—Ph
1-159
5-NHAc-dithia
4-F—Ph
1-160
5-NHAc-oxathia
4-F—Ph
1-161
4,4-diMe-cHex
4-F—Ph
1-162
5,5-diMe-dioxa
4-F—Ph
1-163
5,5-diMe-dithia
4-F—Ph
1-164
5,5-diMe-oxathia
4-F—Ph
1-165
4,4-diHM-cHex
4-F—Ph
1-166
5,5-diHM-dioxa
4-F—Ph
1-167
5,5-diHM-dithia
4-F—Ph
1-168
5,5-diHM-oxathia
4-F—Ph
1-169
ring 15
4-F—Ph
1-170
ring 16
4-F—Ph
1-171
ring 17
4-F—Ph
1-172
ring 18
4-F—Ph
1-173
4,4-diCO2Et-cHex
4-F—Ph
1-174
5,5-diCO2Et-dioxa
4-F—Ph
1-175
5,5-diCO2Et-dithia
4-F—Ph
1-176
5,5-diCO2Et-oxathia
4-F—Ph
1-177
O═
2-Cl—Ph
1-178
S═
2-Cl—Ph
1-179
cPr
2-Cl—Ph
1-180
cBn
2-Cl—Ph
1-181
cPent
2-Cl—Ph
1-182
cHex
2-Cl—Ph
1-183
cHept
2-Cl—Ph
1-184
oxi
2-Cl—Ph
1-185
oxe
2-Cl—Ph
1-186
oxo
2-Cl—Ph
1-187
oxa
2-Cl—Ph
1-188
dioxo
2-Cl—Ph
1-189
dioxa
2-Cl—Ph
1-190
dioxe
2-Cl—Ph
1-191
dithio
2-Cl—Ph
1-192
dithia
2-Cl—Ph
1-193
ring 1
2-Cl—Ph
1-194
ring 2
2-Cl—Ph
1-195
oxathio
2-Cl—Ph
1-196
oxathia
2-Cl—Ph
1-197
ozl
2-Cl—Ph
1-198
ozn
2-Cl—Ph
1-199
tzl
2-Cl—Ph
1-200
tzn
2-Cl—Ph
1-201
3-HM-cPent
2-Cl—Ph
1-202
4-HM-dioxo
2-Cl—Ph
1-203
4-HM-dithio
2-Cl—Ph
1-204
4-HM-oxathio
2-Cl—Ph
1-205
3,4-diHM-cPent
2-Cl—Ph
1-206
4,5-diHM-dioxo
2-Cl—Ph
1-207
4,5-diHM-dithio
2-Cl—Ph
1-208
4,5-diHM-oxathio
2-Cl—Ph
1-209
3,4-diHE-cPent
2-Cl—Ph
1-210
4,5-diHE-dioxo
2-Cl—Ph
1-211
4,5-diHE-dithio
2-Cl—Ph
1-212
4,5-diHE-oxathio
2-Cl—Ph
1-213
3-HE-cPent
2-Cl—Ph
1-214
4-HE-dioxo
2-Cl—Ph
1-215
4-HE-dithio
2-Cl—Ph
1-216
4-HE-oxathio
2-Cl—Ph
1-217
3-HP-cPent
2-Cl—Ph
1-218
4-HP-dioxo
2-Cl—Ph
1-219
4-HP-dithio
2-Cl—Ph
1-220
4-HP-oxathio
2-Cl—Ph
1-221
3-HB-cPent
2-Cl—Ph
1-222
4-HB-dioxo
2-Cl—Ph
1-223
4-HB-dithio
2-Cl—Ph
1-224
4-HB-oxathio
2-Cl—Ph
1-225
ring 3
2-Cl—Ph
1-226
ring 4
2-Cl—Ph
1-227
ring 5
2-Cl—Ph
1-228
ring 6
2-Cl—Ph
1-229
ring 7
2-Cl—Ph
1-230
ring 8
2-Cl—Ph
1-231
ring 9
2-Cl—Ph
1-232
ring 10
2-Cl—Ph
1-233
3,4-diCH2NHAc-cPent
2-Cl—Ph
1-234
4,5-diCH2NHAc-dioxo
2-Cl—Ph
1-235
4,5-diCH2NHAc-dithio
2-Cl—Ph
1-236
4,5-diCH2NHAc-oxathio
2-Cl—Ph
1-237
ring 11
2-Cl—Ph
1-238
ring 12
2-Cl—Ph
1-239
ring 13
2-Cl—Ph
1-240
ring 14
2-Cl—Ph
1-241
4-OH-cHex
2-Cl—Ph
1-242
5-OH-dioxa
2-Cl—Ph
1-243
5-OH-dithia
2-Cl—Ph
1-244
5-OH-oxathia
2-Cl—Ph
1-245
4-NHAc-cHex
2-Cl—Ph
1-246
5-NHAc-dioxa
2-Cl—Ph
1-247
5-NHAc-dithia
2-Cl—Ph
1-248
5-NHAc-oxathia
2-Cl—Ph
1-249
4,4-diMe-cHex
2-Cl—Ph
1-250
5,5-diMe-dioxa
2-Cl—Ph
1-251
5,5-diMe-dithia
2-Cl—Ph
1-252
5,5-diMe-oxathia
2-Cl—Ph
1-253
4,4-diHM-cHex
2-Cl—Ph
1-254
5,5-diHM-dioxa
2-Cl—Ph
1-255
5,5-diHM-dithia
2-Cl—Ph
1-256
5,5-diHM-oxathia
2-Cl—Ph
1-257
ring 15
2-Cl—Ph
1-258
ring 16
2-Cl—Ph
1-259
ring 17
2-Cl—Ph
1-260
ring 18
2-Cl—Ph
1-261
4,4-diCO2Et-cHex
2-Cl—Ph
1-262
5,5-diCO2Et-dioxa
2-Cl—Ph
1-263
5,5-diCO2Et-dithia
2-Cl—Ph
1-264
5,5-diCO2Et-oxathia
2-Cl—Ph
1-265
O═
2,4-diF—Ph
1-266
S═
2,4-diF—Ph
1-267
cPr
2,4-diF—Ph
1-268
cBu
2,4-diF—Ph
1-269
cPent
2,4-diF—Ph
1-270
cHex
2,4-diF—Ph
1-271
cHept
2,4-diF—Ph
1-272
oxi
2,4-diF—Ph
1-273
oxe
2,4-diF—Ph
1-274
oxo
2,4-diF—Ph
1-275
oxa
2,4-diF—Ph
1-276
dioxo
2,4-diF—Ph
1-277
dioxa
2,4-diF—Ph
1-278
dioxe
2,4-diF—Ph
1-279
dithio
2,4-diF—Ph
1-280
dithia
2,4-diF—Ph
1-281
ring 1
2,4-diF—Ph
1-282
ring 2
2,4-diF—Ph
1-283
oxathio
2,4-diF—Ph
1-284
oxathia
2,4-diF—Ph
1-285
ozl
2,4-diF—Ph
1-286
ozn
2,4-diF—Ph
1-287
tzl
2,4-diF—Ph
1-288
tzn
2,4-diF—Ph
1-289
3-HM-cPent
2,4-diF—Ph
1-290
4-HM-dioxo
2,4-diF—Ph
1-291
4-HM-dithio
2,4-diF—Ph
1-292
4-HM-oxathio
2,4-diF—Ph
1-293
3,4-diHM-cPent
2,4-diF—Ph
1-294
4,5-diHM-dioxo
2,4-diF—Ph
1-295
4,5-diHM-dithio
2,4-diF—Ph
1-296
4,5-diHM-oxathio
2,4-diF—Ph
1-297
3,4-diHE-cPent
2,4-diF—Ph
1-298
4,5-diHE-dioxo
2,4-diF—Ph
1-299
4,5-diHE-dithio
2,4-diF—Ph
1-300
4,5-diHE-oxathio
2,4-diF—Ph
1-301
3-HE-cPent
2,4-diF—Ph
1-302
4-HE-dioxo
2,4-diF—Ph
1-303
4-HE-dithio
2,4-diF—Ph
1-304
4-HE-oxathio
2,4-diF—Ph
1-305
3-HP-cPent
2,4-diF—Ph
1-306
4-HP-dioxo
2,4-diF—Ph
1-307
4-HP-dithio
2,4-diF—Ph
1-308
4-HP-oxathio
2,4-diF—Ph
1-309
3-HB-cPent
2,4-diF—Ph
1-310
4-HB-dioxo
2,4-diF—Ph
1-311
4-HB-dithio
2,4-diF—Ph
1-312
4-HB-oxathio
2,4-diF—Ph
1-313
ring 3
2,4-diF—Ph
1-314
ring 4
2,4-diF—Ph
1-315
ring 5
2,4-diF—Ph
1-316
ring 6
2,4-diF—Ph
1-317
ring 7
2,4-diF—Ph
1-318
ring 8
2,4-diF—Ph
1-319
ring 9
2,4-diF—Ph
1-320
ring 10
2,4-diF—Ph
1-321
3,4-diCH2NHAc-cPent
2,4-diF—Ph
1-322
4,5-diCH2NHAc-dioxo
2,4-diF—Ph
1-323
4,5-diCH2NHAc-dithio
2,4-diF—Ph
1-324
4,5-diCH2NHAc-oxathio
2,4-diF—Ph
1-325
ring 11
2,4-diF—Ph
1-326
ring 12
2,4-diF—Ph
1-327
ring 13
2,4-diF—Ph
1-328
ring 14
2,4-diF—Ph
1-329
4-OH-cHex
2,4-diF—Ph
1-330
5-OH-dioxa
2,4-diF—Ph
1-331
5-OH-dithia
2,4-diF—Ph
1-332
5-OH-oxathia
2,4-diF—Ph
1-333
4-NHAc-cHex
2,4-diF—Ph
1-334
5-NHAc-dioxa
2,4-diF—Ph
1-335
5-NHAc-dithia
2,4-diF—Ph
1-336
5-NHAc-oxathia
2,4-diF—Ph
1-337
4,4-diMe-cHex
2,4-diF—Ph
1-338
5,5-diMe-dioxa
2,4-diF—Ph
1-339
5,5-diMe-dithia
2,4-diF—Ph
1-340
5,5-diMe-oxathia
2,4-diF—Ph
1-341
4,4-diHM-cHex
2,4-diF—Ph
1-342
5,5-diHM-dioxa
2,4-diF—Ph
1-343
5,5-diHM-dithia
2,4-diF—Ph
1-344
5,5-diHM-oxathia
2,4-diF—Ph
1-345
ring 15
2,4-diF—Ph
1-346
ring 16
2,4-diF—Ph
1-347
ring 17
2,4-diF—Ph
1-348
ring 18
2,4-diF—Ph
1-349
4,4-diCO2Et-cHex
2,4-diF—Ph
1-350
5,5-diCO2Et-dioxa
2,4-diF—Ph
1-351
5,5-diCO2Et-dithia
2,4-diF—Ph
1-352
5,5-diCO2Et-oxathia
2,4-diF—Ph
1-353
O═
2-Cl-4-F—Ph
1-354
S═
2-Cl-4-F—Ph
1-355
cPr
2-Cl-4-F—Ph
1-356
cBu
2-Cl-4-F—Ph
1-357
cPent
2-Cl-4-F—Ph
1-358
cHex
2-Cl-4-F—Ph
1-359
cHept
2-Cl-4-F—Ph
1-360
oxi
2-Cl-4-F—Ph
1-361
oxe
2-Cl-4-F—Ph
1-362
oxo
2-Cl-4-F—Ph
1-363
oxa
2-Cl-4-F—Ph
1-364
dioxo
2-Cl-4-F—Ph
1-365
dioxa
2-Cl-4-F—Ph
1-366
dioxe
2-Cl-4-F—Ph
1-367
dithio
2-Cl-4-F—Ph
1-368
dithia
2-Cl-4-F—Ph
1-369
ring 1
2-Cl-4-F—Ph
1-370
ring 2
2-Cl-4-F—Ph
1-371
oxathio
2-Cl-4-F—Ph
1-372
oxathia
2-Cl-4-F—Ph
1-373
ozl
2-Cl-4-F—Ph
1-374
ozn
2-Cl-4-F—Ph
1-375
tzl
2-Cl-4-F—Ph
1-376
tzn
2-Cl-4-F—Ph
1-377
3-HM-cPent
2-Cl-4-F—Ph
1-378
4-HM-dioxo
2-Cl-4-F—Ph
1-379
4-HM-dithio
2-Cl-4-F—Ph
1-380
4-HM-oxathio
2-Cl-4-F—Ph
1-381
3,4-diHM-cPent
2-Cl-4-F—Ph
1-382
4,5-diHM-dioxo
2-Cl-4-F—Ph
1-383
4,5-diHM-dithio
2-Cl-4-F—Ph
1-384
4,5-diHM-oxathio
2-Cl-4-F—Ph
1-385
3,4-diHE-cPent
2-Cl-4-F—Ph
1-386
4,5-diHE-dioxo
2-Cl-4-F—Ph
1-387
4,5-diHE-dithio
2-Cl-4-F—Ph
1-388
4,5-diHE-oxathio
2-Cl-4-F—Ph
1-389
3-HE-cPent
2-Cl-4-F—Ph
1-390
4-HE-dioxo
2-Cl-4-F—Ph
1-391
4-HE-dithio
2-Cl-4-F—Ph
1-392
4-HE-oxathio
2-Cl-4-F—Ph
1-393
3-HP-cPent
2-Cl-4-F—Ph
1-394
4-HP-dioxo
2-Cl-4-F—Ph
1-395
4-HP-dithio
2-Cl-4-F—Ph
1-396
4-HP-oxathio
2-Cl-4-F—Ph
1-397
3-HB-cPent
2-Cl-4-F—Ph
1-398
4-HB-dioxo
2-Cl-4-F—Ph
1-399
4-HB-dithio
2-Cl-4-F—Ph
1-400
4-HB-oxathio
2-Cl-4-F—Ph
1-401
ring 3
2-Cl-4-F—Ph
1-402
ring 4
2-Cl-4-F—Ph
1-403
ring 5
2-Cl-4-F—Ph
1-404
ring 6
2-Cl-4-F—Ph
1-405
ring 7
2-Cl-4-F—Ph
1-406
ring 8
2-Cl-4-F—Ph
1-407
ring 9
2-Cl-4-F—Ph
1-408
ring 10
2-Cl-4-F—Ph
1-409
3,4-diCH2NHAc-cPent
2-Cl-4-F—Ph
1-410
4,5-diCH2NHAc-dioxo
2-Cl-4-F—Ph
1-411
4,5-diCH2NHAc-dithio
2-Cl-4-F—Ph
1-412
4,5-diCH2NHAc-oxathio
2-Cl-4-F—Ph
1-413
ring 11
2-Cl-4-F—Ph
1-414
ring 12
2-Cl-4-F—Ph
1-415
ring 13
2-Cl-4-F—Ph
1-416
ring 14
2-Cl-4-F—Ph
1-417
4-OH-cHex
2-Cl-4-F—Ph
1-418
5-OH-dioxa
2-Cl-4-F—Ph
1-419
5-OH-dithia
2-Cl-4-F—Ph
1-420
5-OH-oxathia
2-Cl-4-F—Ph
1-421
4-NHAc-cHex
2-Cl-4-F—Ph
1-422
5-NHAc-dioxa
2-Cl-4-F—Ph
1-423
5-NHAc-dithia
2-Cl-4-F—Ph
1-424
5-NHAc-oxathia
2-Cl-4-F—Ph
1-425
4,4-diMe-cHex
2-Cl-4-F—Ph
1-426
5,5-diMe-dioxa
2-Cl-4-F—Ph
1-427
5,5-diMe-dithia
2-Cl-4-F—Ph
1-428
5,5-diMe-oxathia
2-Cl-4-F—Ph
1-429
4,4-diHM-cHex
2-Cl-4-F—Ph
1-430
5,5-diHM-dioxa
2-Cl-4-F—Ph
1-431
5,5-diHM-dithia
2-Cl-4-F—Ph
1-432
5,5-diHM-oxathia
2-Cl-4-F—Ph
1-433
ring 15
2-Cl-4-F—Ph
1-434
ring 16
2-Cl-4-F—Ph
1-435
ring 17
2-Cl-4-F—Ph
1-436
ring 18
2-Cl-4-F—Ph
1-437
4,4-diCO2Et-cHex
2-Cl-4-F—Ph
1-438
5,5-diCO2Et-dioxa
2-Cl-4-F—Ph
1-439
5,5-diCO2Et-dithia
2-Cl-4-F—Ph
1-440
5,5-diCO2Et-oxathia
2-Cl-4-F—Ph
1-441
O═
2-Cl-4-Me—Ph
1-442
S═
2-Cl-4-Me—Ph
1-443
cPr
2-Cl-4-Me—Ph
1-444
cBu
2-Cl-4-Me—Ph
1-445
cPent
2-Cl-4-Me—Ph
1-446
cHex
2-Cl-4-Me—Ph
1-447
cHept
2-Cl-4-Me—Ph
1-448
oxi
2-Cl-4-Me—Ph
1-449
oxe
2-Cl-4-Me—Ph
1-450
oxo
2-Cl-4-Me—Ph
1-451
oxa
2-Cl-4-Me—Ph
1-452
dioxo
2-Cl-4-Me—Ph
1-453
dioxa
2-Cl-4-Me—Ph
1-454
dioxe
2-Cl-4-Me—Ph
1-455
dithio
2-Cl-4-Me—Ph
1-456
dithia
2-Cl-4-Me—Ph
1-457
ring 1
2-Cl-4-Me—Ph
1-458
ring 2
2-Cl-4-Me—Ph
1-459
oxathio
2-Cl-4-Me—Ph
1-460
oxathia
2-Cl-4-Me—Ph
1-461
ozl
2-Cl-4-Me—Ph
1-462
ozn
2-Cl-4-Me—Ph
1-463
tzl
2-Cl-4-Me—Ph
1-464
tzn
2-Cl-4-Me—Ph
1-465
3-HM-cPent
2-Cl-4-Me—Ph
1-466
4-HM-dioxo
2-Cl-4-Me—Ph
1-467
4-HM-dithio
2-Cl-4-Me—Ph
1-468
4-HM-oxathio
2-Cl-4-Me—Ph
1-469
3,4-diHM-cPent
2-Cl-4-Me—Ph
1-470
4,5-diHM-dioxo
2-Cl-4-Me—Ph
1-471
4,5-diHM-dithio
2-Cl-4-Me—Ph
1-472
4,5-diHM-oxathio
2-Cl-4-Me—Ph
1-473
3,4-diHE-cPent
2-Cl-4-Me—Ph
1-474
4,5-diHE-dioxo
2-Cl-4-Me—Ph
1-475
4,5-diHE-dithio
2-Cl-4-Me—Ph
1-476
4,5-diHE-oxathio
2-Cl-4-Me—Ph
1-477
3-HE-cPent
2-Cl-4-Me—Ph
1-478
4-HE-dioxo
2-Cl-4-Me—Ph
1-479
4-HE-dithio
2-Cl-4-Me—Ph
1-480
4-HE-oxathio
2-Cl-4-Me—Ph
1-481
3-HP-cPent
2-Cl-4-Me—Ph
1-482
4-HP-dioxo
2-Cl-4-Me—Ph
1-483
4-HP-dithio
2-Cl-4-Me—Ph
1-484
4-HP-oxathio
2-Cl-4-Me—Ph
1-485
3-HB-cPent
2-Cl-4-Me—Ph
1-486
4-HB-dioxo
2-Cl-4-Me—Ph
1-487
4-HB-dithio
2-Cl-4-Me—Ph
1-488
4-HB-oxathio
2-Cl-4-Me—Ph
1-489
ring 3
2-Cl-4-Me—Ph
1-490
ring 4
2-Cl-4-Me—Ph
1-491
ring 5
2-Cl-4-Me—Ph
1-492
ring 6
2-Cl-4-Me—Ph
1-493
ring 7
2-Cl-4-Me—Ph
1-494
ring 8
2-Cl-4-Me—Ph
1-495
ring 9
2-Cl-4-Me—Ph
1-496
ring 10
2-Cl-4-Me—Ph
1-497
3,4-diCH2NHAc-cPent
2-Cl-4-Me—Ph
1-498
4,5-diCH2NHAc-dioxo
2-Cl-4-Me—Ph
1-499
4,5-diCH2NHAc-dithio
2-Cl-4-Me—Ph
1-500
4,5-diCH2NHAc-oxathio
2-Cl-4-Me—Ph
1-501
ring 11
2-Cl-4-Me—Ph
1-502
ring 12
2-Cl-4-Me—Ph
1-503
ring 13
2-Cl-4-Me—Ph
1-504
ring 14
2-Cl-4-Me—Ph
1-505
4-OH-cHex
2-Cl-4-Me—Ph
1-506
5-OH-dioxa
2-Cl-4-Me—Ph
1-507
5-OH-dithia
2-Cl-4-Me—Ph
1-508
5-OH-oxathia
2-Cl-4-Me—Ph
1-509
4-NHAc-cHex
2-Cl-4-Me—Ph
1-510
5-NHAc-dioxa
2-Cl-4-Me—Ph
1-511
5-NHAc-dithia
2-Cl-4-Me—Ph
1-512
5-NHAc-oxathia
2-Cl-4-Me—Ph
1-513
4,4-diMe-cHex
2-Cl-4-Me—Ph
1-514
5,5-diMe-dioxa
2-Cl-4-Me—Ph
1-515
5,5-diMe-dithia
2-Cl-4-Me—Ph
1-516
5,5-diMe-oxathia
2-Cl-4-Me—Ph
1-517
4,4-diHM-cHex
2-Cl-4-Me—Ph
1-518
5,5-diHM-dioxa
2-Cl-4-Me—Ph
1-519
5,5-diHM-dithia
2-Cl-4-Me—Ph
1-520
5,5-diHM-oxathia
2-Cl-4-Me—Ph
1-521
ring 15
2-Cl-4-Me—Ph
1-522
ring 16
2-Cl-4-Me—Ph
1-523
ring 17
2-Cl-4-Me—Ph
1-524
ring 18
2-Cl-4-Me—Ph
1-525
4,4-diCO2Et-cHex
2-Cl-4-Me—Ph
1-526
5,5-diCO2Et-dioxa
2-Cl-4-Me—Ph
1-527
5,5-diCO2Et-dithia
2-Cl-4-Me—Ph
1-528
5,5-diCO2Et-oxathia
2-Cl-4-Me—Ph
1-529
O═
2-nBu—Ph
1-530
S═
2-nBu—Ph
1-531
cPr
2-nBu—Ph
1-532
cBu
2-nBu—Ph
1-533
cPent
2-nBu—Ph
1-534
cHex
2-nBu—Ph
1-535
cHept
2-nBu—Ph
1-536
oxi
2-nBu—Ph
1-537
oxe
2-nBu—Ph
1-538
oxo
2-nBu—Ph
1-539
oxa
2-nBu—Ph
1-540
dioxo
2-nBu—Ph
1-541
dioxa
2-nBu—Ph
1-542
dioxe
2-nBu—Ph
1-543
dithio
2-nBu—Ph
1-544
dithia
2-nBu—Ph
1-545
ring 1
2-nBu—Ph
1-546
ring 2
2-nBu—Ph
1-547
oxathio
2-nBu—Ph
1-548
oxathia
2-nBu—Ph
1-549
ozl
2-nBu—Ph
1-550
ozn
2-nBu—Ph
1-551
tzl
2-nBu—Ph
1-552
tzn
2-nBu—Ph
1-553
3-HM-cPent
2-nBu—Ph
1-554
4-HM-dioxo
2-nBu—Ph
1-555
4-HM-dithio
2-nBu—Ph
1-556
4-HM-oxathio
2-nBu—Ph
1-557
3,4-diHM-cPent
2-nBu—Ph
1-558
4,5-diHM-dioxo
2-nBu—Ph
1-559
4,5-diHM-dithio
2-nBu—Ph
1-560
4,5-diHM-oxathio
2-nBu—Ph
1-561
3,4-diHE-cPent
2-nBu—Ph
1-562
4,5-diHE-dioxo
2-nBu—Ph
1-563
4,5-diHE-dithio
2-nBu—Ph
1-564
4,5-diHE-oxathio
2-nBu—Ph
1-565
3-HE-cPent
2-nBu—Ph
1-566
4-HE-dioxo
2-nBu—Ph
1-567
4-HE-dithio
2-nBu—Ph
1-568
4-HE-oxathio
2-nBu—Ph
1-569
3-HP-cPent
2-nBu—Ph
1-570
4-HP-dioxo
2-nBu—Ph
1-571
4-HP-dithio
2-nBu—Ph
1-572
4-HP-oxathio
2-nBu—Ph
1-573
3-HB-cPent
2-nBu—Ph
1-574
4-HB-dioxo
2-nBu—Ph
1-575
4-HB-dithio
2-nBu—Ph
1-576
4-HB-oxathio
2-nBu—Ph
1-577
ring 3
2-nBu—Ph
1-578
ring 4
2-nBu—Ph
1-579
ring 5
2-nBu—Ph
1-580
ring 6
2-nBu—Ph
1-581
ring 7
2-nBu—Ph
1-582
ring 8
2-nBu—Ph
1-583
ring 9
2-nBu—Ph
1-584
ring 10
2-nBu—Ph
1-585
3,4-diCH2NHAc-cPent
2-nBu—Ph
1-586
4,5-diCH2NHAc-dioxo
2-nBu—Ph
1-587
4,5-diCH2NHAc-dithio
2-nBu—Ph
1-588
4,5-diCH2NHAc-oxathio
2-nBu—Ph
1-589
ring 11
2-nBu—Ph
1-590
ring 12
2-nBu—Ph
1-591
ring 13
2-nBu—Ph
1-592
ring 14
2-nBu—Ph
1-593
4-OH-cHex
2-nBu—Ph
1-594
5-OH-dioxa
2-nBu—Ph
1-595
5-OH-dithia
2-nBu—Ph
1-596
5-OH-oxathia
2-nBu—Ph
1-597
4-NHAc-cHex
2-nBu—Ph
1-598
5-NHAc-dioxa
2-nBu—Ph
1-599
5-NHAc-dithia
2-nBu—Ph
1-600
5-NHAc-oxathia
2-nBu—Ph
1-601
4,4-diMe-cHex
2-nBu—Ph
1-602
5,5-diMe-dioxa
2-nBu—Ph
1-603
5,5-diMe-dithia
2-nBu—Ph
1-604
5,5-diMe-oxathia
2-nBu—Ph
1-605
4,4-diHM-cHex
2-nBu—Ph
1-606
5,5-diHM-dioxa
2-nBu—Ph
1-607
5,5-diHM-dithia
2-nBu—Ph
1-608
5,5-diHM-oxathia
2-nBu—Ph
1-609
ring 15
2-nBu—Ph
1-610
ring 16
2-nBu—Ph
1-611
ring 17
2-nBu—Ph
1-612
ring 18
2-nBu—Ph
1-612
4,4-diCO2Et-cHex
2-nBu—Ph
1-614
5,5-diCO2Et-dioxa
2-nBu—Ph
1-615
5,5-diCO2Et-dithia
2-nBu—Ph
1-616
5,5-diCO2Et-oxathia
2-nBu—Ph
1-617
O═
2-nBu-4-F—Ph
1-618
S═
2-nBu-4-F—Ph
1-619
cPr
2-nBu-4-F—Ph
1-620
cBu
2-nBu-4-F—Ph
1-621
cPent
2-nBu-4-F—Ph
1-622
cHex
2-nBu-4-F—Ph
1-623
cHept
2-nBu-4-F—Ph
1-624
oxi
2-nBu-4-F—Ph
1-625
oxe
2-nBu-4-F—Ph
1-626
oxo
2-nBu-4-F—Ph
1-627
oxa
2-nBu-4-F—Ph
1-628
dioxo
2-nBu-4-F—Ph
1-629
dioxa
2-nBu-4-F—Ph
1-630
dioxe
2-nBu-4-F—Ph
1-631
dithio
2-nBu-4-F—Ph
1-632
dithia
2-nBu-4-F—Ph
1-633
ring 1
2-nBu-4-F—Ph
1-634
ring 2
2-nBu-4-F—Ph
1-635
oxathio
2-nBu-4-F—Ph
1-636
oxathia
2-nBu-4-F—Ph
1-637
ozl
2-nBu-4-F—Ph
1-638
ozn
2-nBu-4-F—Ph
1-639
tzl
2-nBu-4-F—Ph
1-640
tzn
2-nBu-4-F—Ph
1-641
3-HM-cPent
2-nBu-4-F—Ph
1-642
4-HM-dioxo
2-nBu-4-F—Ph
1-643
4-HM-dithio
2-nBu-4-F—Ph
1-644
4-HM-oxathio
2-nBu-4-F—Ph
1-645
3,4-diHM-cPent
2-nBu-4-F—Ph
1-646
4,5-diHM-dioxo
2-nBu-4-F—Ph
1-647
4,5-diHM-dithio
2-nBu-4-F—Ph
1-648
4,5-diHM-oxathio
2-nBu-4-F—Ph
1-649
3,4-diHE-cPent
2-nBu-4-F—Ph
1-650
4,5-diHE-dioxo
2-nBu-4-F—Ph
1-651
4,5-diHE-dithio
2-nBu-4-F—Ph
1-652
4,5-diHE-oxathio
2-nBu-4-F—Ph
1-653
3-HE-cPent
2-nBu-4-F—Ph
1-654
4-HE-dioxo
2-nBu-4-F—Ph
1-655
4-HE-dithio
2-nBu-4-F—Ph
1-656
4-HE-oxathio
2-nBu-4-F—Ph
1-657
3-HP-cPent
2-nBu-4-F—Ph
1-658
4-HP-dioxo
2-nBu-4-F—Ph
1-659
4-HP-dithio
2-nBu-4-F—Ph
1-660
4-HP-oxathio
2-nBu-4-F—Ph
1-661
3-HB-cPent
2-nBu-4-F—Ph
1-662
4-HB-dioxo
2-nBu-4-F—Ph
1-663
4-HB-dithio
2-nBu-4-F—Ph
1-664
4-HB-oxathio
2-nBu-4-F—Ph
1-665
ring 3
2-nBu-4-F—Ph
1-666
ring 4
2-nBu-4-F—Ph
1-667
ring 5
2-nBu-4-F—Ph
1-668
ring 6
2-nBu-4-F—Ph
1-669
ring 7
2-nBu-4-F—Ph
1-670
ring 8
2-nBu-4-F—Ph
1-671
ring 9
2-nBu-4-F—Ph
1-672
ring 10
2-nBu-4-F—Ph
1-673
3,4-diCH2NHAc-cPent
2-nBu-4-F—Ph
1-674
4,5-diCH2NHAc-dioxo
2-nBu-4-F—Ph
1-675
4,5-diCH2NHAc-dithio
2-nBu-4-F—Ph
1-676
4,5-diCH2NHAc-oxathio
2-nBu-4-F—Ph
1-677
ring 11
2-nBu-4-F—Ph
1-678
ring 12
2-nBu-4-F—Ph
1-679
ring 13
2-nBu-4-F—Ph
1-680
ring 14
2-nBu-4-F—Ph
1-681
4-OH-cHex
2-nBu-4-F—Ph
1-682
5-OH-dioxa
2-nBu-4-F—Ph
1-683
5-OH-dithia
2-nBu-4-F—Ph
1-684
5-OH-oxathia
2-nBu-4-F—Ph
1-685
4-NHAc-cHex
2-nBu-4-F—Ph
1-686
5-NHAc-dioxa
2-nBu-4-F—Ph
1-687
5-NHAc-dithia
2-nBu-4-F—Ph
1-688
5-NHAc-oxathia
2-nBu-4-F—Ph
1-689
4,4-diMe-cHex
2-nBu-4-F—Ph
1-690
5,5-diMe-dioxa
2-nBu-4-F—Ph
1-691
5,5-diMe-dithia
2-nBu-4-F—Ph
1-692
5,5-diMe-oxathia
2-nBu-4-F—Ph
1-693
4,4-diHM-cHex
2-nBu-4-F—Ph
1-694
5,5-diHM-dioxa
2-nBu-4-F—Ph
1-695
5,5-diHM-dithia
2-nBu-4-F—Ph
1-696
5,5-diHM-oxathia
2-nBu-4-F—Ph
1-697
ring 15
2-nBu-4-F—Ph
1-698
ring 16
2-nBu-4-F—Ph
1-699
ring 17
2-nBu-4-F—Ph
1-700
ring 18
2-nBu-4-F—Ph
1-701
4,4-diCO2Et-cHex
2-nBu-4-F—Ph
1-702
5,5-diCO2Et-dioxa
2-nBu-4-F—Ph
1-703
5,5-diCO2Et-dithia
2-nBu-4-F—Ph
1-704
5,5-diCO2Et-oxathia
2-nBu-4-F—Ph
1-705
O═
2-nHex—Ph
1-706
S═
2-nHex—Ph
1-707
cPr
2-nHex—Ph
1-708
cBu
2-nHex—Ph
1-709
cPent
2-nHex—Ph
1-710
cHex
2-nHex—Ph
1-711
cHept
2-nHex—Ph
1-712
oxi
2-nHex—Ph
1-713
oxe
2-nHex—Ph
1-714
oxo
2-nHex—Ph
1-715
oxa
2-nHex—Ph
1-716
dioxo
2-nHex—Ph
1-717
dioxa
2-nHex—Ph
1-718
dioxe
2-nHex—Ph
1-719
dithio
2-nHex—Ph
1-720
dithia
2-nHex—Ph
1-721
ring 1
2-nHex—Ph
1-722
ring 2
2-nHex—Ph
1-723
oxathio
2-nHex—Ph
1-724
oxathia
2-nHex—Ph
1-725
ozl
2-nHex—Ph
1-726
ozn
2-nHex—Ph
1-727
tzl
2-nHex—Ph
1-728
tzn
2-nHex—Ph
1-729
3-HM-cPent
2-nHex—Ph
1-730
4-HM-dioxo
2-nHex—Ph
1-731
4-HM-dithio
2-nHex—Ph
1-732
4-HM-oxathio
2-nHex—Ph
1-733
3,4-diHM-cPent
2-nHex—Ph
1-734
4,5-diHM-dioxo
2-nHex—Ph
1-735
4,5-diHM-dithio
2-nHex—Ph
1-736
4,5-diHM-oxathio
2-nHex—Ph
1-737
3,4-diHE-cPent
2-nHex—Ph
1-738
4,5-diHE-dioxo
2-nHex—Ph
1-739
4,5-diHE-dithio
2-nHex—Ph
1-740
4,5-diHE-oxathio
2-nHex—Ph
1-741
3-HE-cPent
2-nHex—Ph
1-742
4-HE-dioxo
2-nHex—Ph
1-743
4-HE-dithio
2-nHex—Ph
1-744
4-HE-oxathio
2-nHex—Ph
1-745
3-HP-cPent
2-nHex—Ph
1-746
4-HP-dioxo
2-nHex—Ph
1-747
4-HP-dithio
2-nHex—Ph
1-748
4-HP-oxathio
2-nHex—Ph
1-749
3-HB-cPent
2-nHex—Ph
1-750
4-HB-dioxo
2-nHex—Ph
1-751
4-HB-dithio
2-nHex—Ph
1-752
4-HB-oxathio
2-nHex—Ph
1-753
ring 3
2-nHex—Ph
1-754
ring 4
2-nHex—Ph
1-755
ring 5
2-nHex—Ph
1-756
ring 6
2-nHex—Ph
1-757
ring 7
2-nHex—Ph
1-758
ring 8
2-nHex—Ph
1-759
ring 9
2-nHex—Ph
1-760
ring 10
2-nHex—Ph
1-761
3,4-diCH2NHAc-cPent
2-nHex—Ph
1-762
4,5-diCH2NHAc-dioxo
2-nHex—Ph
1-763
4,5-diCH2NHAc-dithio
2-nHex—Ph
1-764
4,5-diCH2NHAc-oxathio
2-nHex—Ph
1-765
ring 11
2-nHex—Ph
1-766
ring 12
2-nHex—Ph
1-767
ring 13
2-nHex—Ph
1-768
ring 14
2-nHex—Ph
1-769
4-OH-cHex
2-nHex—Ph
1-770
5-OH-dioxa
2-nHex—Ph
1-771
5-OH-dithia
2-nHex—Ph
1-772
5-OH-oxathia
2-nHex—Ph
1-773
4-NHAc-cHex
2-nHex—Ph
1-774
5-NHAc-dioxa
2-nHex—Ph
1-775
5-NHAc-dithia
2-nHex—Ph
1-776
5-NHAc-oxathia
2-nHex—Ph
1-777
4,4-diMe-cHex
2-nHex—Ph
1-778
5,5-diMe-dioxa
2-nHex—Ph
1-779
5,5-diMe-dithia
2-nHex—Ph
1-780
5,5-diMe-oxathia
2-nHex—Ph
1-781
4,4-diHM-cHex
2-nHex—Ph
1-782
5,5-diHM-dioxa
2-nHex—Ph
1-783
5,5-diHM-dithia
2-nHex—Ph
1-784
5,5-diHM-oxathia
2-nHex—Ph
1-785
ring 15
2-nHex—Ph
1-786
ring 16
2-nHex—Ph
1-787
ring 17
2-nHex—Ph
1-788
ring 18
2-nHex—Ph
1-789
4,4-diCO2Et-cHex
2-nHex—Ph
1-790
5,5-diCO2Et-dioxa
2-nHex—Ph
1-791
5,5-diCO2Et-dithia
2-nHex—Ph
1-792
5,5-diCO2Et-oxathia
2-nHex—Ph
1-793
O═
4-F-2-nHex—Ph
1-794
S═
4-F-2-nHex—Ph
1-795
cPr
4-F-2-nHex—Ph
1-796
cBu
4-F-2-nHex—Ph
1-797
cPent
4-F-2-nHex—Ph
1-798
cHex
4-F-2-nHex—Ph
1-799
cHept
4-F-2-nHex—Ph
1-800
oxi
4-F-2-nHex—Ph
1-801
oxe
4-F-2-nHex—Ph
1-802
oxo
4-F-2-nHex—Ph
1-803
oxa
4-F-2-nHex—Ph
1-804
dioxo
4-F-2-nHex—Ph
1-805
dioxa
4-F-2-nHex—Ph
1-806
dioxe
4-F-2-nHex—Ph
1-807
dithio
4-F-2-nHex—Ph
1-808
dithia
4-F-2-nHex—Ph
1-809
ring 1
4-F-2-nHex—Ph
1-810
ring 2
4-F-2-nHex—Ph
1-811
oxathio
4-F-2-nHex—Ph
1-812
oxathia
4-F-2-nHex—Ph
1-813
ozl
4-F-2-nHex—Ph
1-814
ozn
4-F-2-nHex—Ph
1-815
tzl
4-F-2-nHex—Ph
1-816
tzn
4-F-2-nHex—Ph
1-817
3-HM-cPent
4-F-2-nHex—Ph
1-818
4-HM-dioxo
4-F-2-nHex—Ph
1-819
4-HM-dithio
4-F-2-nHex—Ph
1-820
4-HM-oxathio
4-F-2-nHex—Ph
1-821
3,4-diHM-cPent
4-F-2-nHex—Ph
1-822
4,5-diHM-dioxo
4-F-2-nHex—Ph
1-823
4,5-diHM-dithio
4-F-2-nHex—Ph
1-824
4,5-diHM-oxathio
4-F-2-nHex—Ph
1-825
3,4-diHE-cPent
4-F-2-nHex—Ph
1-826
4,5-diHE-dioxo
4-F-2-nHex—Ph
1-827
4,5-diHE-dithio
4-F-2-nHex—Ph
1-828
4,5-diHE-oxathio
4-F-2-nHex—Ph
1-829
3-HE-cPent
4-F-2-nHex—Ph
1-830
4-HE-dioxo
4-F-2-nHex—Ph
1-831
4-HE-dithio
4-F-2-nHex—Ph
1-832
4-HE-oxathio
4-F-2-nHex—Ph
1-833
3-HP-cPent
4-F-2-nHex—Ph
1-834
4-HP-dioxo
4-F-2-nHex—Ph
1-835
4-HP-dithio
4-F-2-nHex—Ph
1-836
4-HP-oxathio
4-F-2-nHex—Ph
1-837
3-HB-cPent
4-F-2-nHex—Ph
1-838
4-HB-dioxo
4-F-2-nHex—Ph
1-839
4-HB-dithio
4-F-2-nHex—Ph
1-840
4-HB-oxathio
4-F-2-nHex—Ph
1-841
ring 3
4-F-2-nHex—Ph
1-842
ring 4
4-F-2-nHex—Ph
1-843
ring 5
4-F-2-nHex—Ph
1-844
ring 6
4-F-2-nHex—Ph
1-845
ring 7
4-F-2-nHex—Ph
1-846
ring 8
4-F-2-nHex—Ph
1-847
ring 9
4-F-2-nHex—Ph
1-848
ring 10
4-F-2-nHex—Ph
1-849
3,4-diCH2NHAc-cPent
4-F-2-nHex—Ph
1-850
4,5-diCH2NHAc-dioxo
4-F-2-nHex—Ph
1-851
4,5-diCH2NHAc-dithio
4-F-2-nHex—Ph
1-852
4,5-diCH2NHAc-oxathio
4-F-2-nHex—Ph
1-853
ring 11
4-F-2-nHex—Ph
1-854
ring 12
4-F-2-nHex—Ph
1-855
ring 13
4-F-2-nHex—Ph
1-856
ring 14
4-F-2-nHex—Ph
1-857
4-OH-cHex
4-F-2-nHex—Ph
1-858
5-OH-dioxa
4-F-2-nHex—Ph
1-859
5-OH-dithia
4-F-2-nHex—Ph
1-860
5-OH-oxathia
4-F-2-nHex—Ph
1-851
4-NHAc-cHex
4-F-2-nHex—Ph
1-852
5-NHAc-dioxa
4-F-2-nHex—Ph
1-863
5-NHAc-dithia
4-F-2-nHex—Ph
1-854
5-NHAc-oxathia
4-F-2-nHex—Ph
1-865
4,4-diMe-cHex
4-F-2-nHex—Ph
1-866
5,5-diMe-dioxa
4-F-2-nHex—Ph
1-857
5,5-diMe-dithia
4-F-2-nHex—Ph
1-868
5,5-diMe-oxathia
4-F-2-nHex—Ph
1-869
4,4-diHM-cHex
4-F-2-nHex—Ph
1-870
5,5-diHM-dioxa
4-F-2-nHex—Ph
1-871
5,5-diHM-dithia
4-F-2-nHex—Ph
1-872
5,5-diHM-oxathia
4-F-2-nHex—Ph
1-873
ring 15
4-F-2-nHex—Ph
1-874
ring 16
4-F-2-nHex—Ph
1-875
ring 17
4-F-2-nHex—Ph
1-876
ring 18
4-F-2-nHex—Ph
1-877
4,4-diCO2Et-cHex
4-F-2-nHex—Ph
1-878
5,5-diCO2Et-dioxa
4-F-2-nHex—Ph
1-879
5,5-diCO2Et-dithia
4-F-2-nHex—Ph
1-880
5,5-diCO2Et-oxathia
4-F-2-nHex—Ph
1-881
O═
2-nHept-Ph
1-882
S═
2-nHept-Ph
1-883
cPr
2-nHept-Ph
1-884
cBu
2-nHept-Ph
1-885
cPent
2-nHept-Ph
1-886
cHex
2-nHept-Ph
1-887
cHept
2-nHept-Ph
1-888
oxi
2-nHept-Ph
1-889
oxe
2-nHept-Ph
1-890
oxo
2-nHept-Ph
1-891
oxa
2-nHept-Ph
1-892
dioxo
2-nHept-Ph
1-893
dioxa
2-nHept-Ph
1-894
dioxe
2-nHept-Ph
1-895
dithio
2-nHept-Ph
1-896
dithia
2-nHept-Ph
1-897
ring 1
2-nHept-Ph
1-898
ring 2
2-nHept-Ph
1-899
oxathio
2-nHept-Ph
1-900
oxathia
2-nHept-Ph
1-901
ozl
2-nHept-Ph
1-902
ozn
2-nHept-Ph
1-903
tzl
2-nHept-Ph
1-904
tzn
2-nHept-Ph
1-905
3-HM-cPent
2-nHept-Ph
1-906
4-HM-dioxo
2-nHept-Ph
1-907
4-HM-dithio
2-nHept-Ph
1-908
4-HM-oxathio
2-nHept-Ph
1-909
3,4-diHM-cPent
2-nHept-Ph
1-910
4,5-diHM-dioxo
2-nHept-Ph
1-911
4,5-diHM-dithio
2-nHept-Ph
1-912
4,5-diHM-oxathio
2-nHept-Ph
1-913
3,4-diHE-cPent
2-nHept-Ph
1-914
4,5-diHE-dioxo
2-nHept-Ph
1-915
4,5-diHE-dithio
2-nHept-Ph
1-916
4,5-diHE-oxathio
2-nHept-Ph
1-917
3-HE-cPent
2-nHept-Ph
1-918
4-HE-dioxo
2-nHept-Ph
1-919
4-HE-dithio
2-nHept-Ph
1-920
4-HE-oxathio
2-nHept-Ph
1-921
3-HP-cPent
2-nHept-Ph
1-922
4-HP-dioxo
2-nHept-Ph
1-923
4-HP-dithio
2-nHept-Ph
1-924
4-HP-oxathio
2-nHept-Ph
1-925
3-HB-oPent
2-nHept-Ph
1-926
4-HB-dioxo
2-nHept-Ph
1-927
4-HB-dithio
2-nHept-Ph
1-928
4-HB-oxathio
2-nHept-Ph
1-929
ring 3
2-nHept-Ph
1-930
ring 4
2-nHept-Ph
1-931
ring 5
2-nHept-Ph
1-932
ring 6
2-nHept-Ph
1-933
ring 7
2-nHept-Ph
1-934
ring 8
2-nHept-Ph
1-935
ring 9
2-nHept-Ph
1-936
ring 10
2-nHept-Ph
1-937
3,4-diCH2NHAc-cPent
2-nHept-Ph
1-938
4,5-diCH2NHAc-dioxo
2-nHept-Ph
1-939
4,5-diCH2NHAc-dithio
2-nHept-Ph
1-940
4,5-diCH2NHAc-oxathi
2-nHept-Ph
1-941
ring 11
2-nHept-Ph
1-942
ring 12
2-nHept-Ph
1-943
ring 13
2-nHept-Ph
1-944
ring 14
2-nHept-Ph
1-945
4-OH-cHex
2-nHept-Ph
1-946
5-OH-dioxa
2-nHept-Ph
1-947
5-OH-dithia
2-nHept-Ph
1-948
5-OH-oxathia
2-nHept-Ph
1-949
4-NHAc-cHex
2-nHept-Ph
1-950
5-NHAc-dioxa
2-nHept-Ph
1-951
5-NHAc-dithia
2-nHept-Ph
1-952
5-NHAc-oxathia
2-nHept-Ph
1-953
4,4-diMe-cHex
2-nHept-Ph
1-954
5,5-diMe-dioxa
2-nHept-Ph
1-955
5,5-diMe-dithia
2-nHept-Ph
1-956
5,5-diMe-oxathia
2-nHept-Ph
1-957
4,4-diHM-cHex
2-nHept-Ph
1-958
5,5-diHM-dioxa
2-nHept-Ph
1-959
5,5-diHM-dithia
2-nHept-Ph
1-960
5,5-diHM-oxathia
2-nHept-Ph
1-961
ring 15
2-nHept-Ph
1-962
ring 16
2-nHept-Ph
1-963
ring 17
2-nHept-Ph
1-964
ring 18
2-nHept-Ph
1-965
4,4-diCO2Et-cHex
2-nHept-Ph
1-966
5,5-diCO2Et-dioxa
2-nHept-Ph
1-967
5,5-diCO2Et-dithia
2-nHept-Ph
1-968
5,5-diCO2Et-oxathia
2-nHept-Ph
1-969
O═
4-F-2-nHept-Ph
1-970
S═
4-F-2-nHept-Ph
1-971
cPr
4-F-2-nHept-Ph
1-972
cBu
4-F-2-nHept-Ph
1-973
cPent
4-F-2-nHept-Ph
1-974
cHex
4-F-2-nHept-Ph
1-975
cHept
4-F-2-nHept-Ph
1-976
oxi
4-F-2-nHept-Ph
1-977
oxe
4-F-2-nHept-Ph
1-978
oxo
4-F-2-nHept-Ph
1-979
oxa
4-F-2-nHept-Ph
1-980
dioxo
4-F-2-nHept-Ph
1-981
dioxa
4-F-2-nHept-Ph
1-982
dioxe
4-F-2-nHept-Ph
1-983
dithio
4-F-2-nHept-Ph
1-984
dithia
4-F-2-nHept-Ph
1-985
ring 1
4-F-2-nHept-Ph
1-986
ring 2
4-F-2-nHept-Ph
1-987
oxathio
4-F-2-nHept-Ph
1-988
oxathia
4-F-2-nHept-Ph
1-989
ozl
4-F-2-nHept-Ph
1-990
ozn
4-F-2-nHept-Ph
1-991
tzl
4-F-2-nHept-Ph
1-992
tzn
4-F-2-nHept-Ph
1-993
3-HM-cPent
4-F-2-nHept-Ph
1-994
4-HM-dioxo
4-F-2-nHept-Ph
1-995
4-HM-dithio
4-F-2-nHept-Ph
1-996
4-HM-oxathio
4-F-2-nHept-Ph
1-997
3,4-diHM-cPent
4-F-2-nHept-Ph
1-998
4,5-diHM-dioxo
4-F-2-nHept-Ph
1-999
4,5-diHM-dithio
4-F-2-nHept-Ph
1-1000
4,5-diHM-oxathio
4-F-2-nHept-Ph
1-1001
3,4-diHE-cPent
4-F-2-nHept-Ph
1-1002
4,5-diHE-dioxo
4-F-2-nHept-Ph
1-1003
4,5-diHE-dithio
4-F-2-nHept-Ph
1-1004
4,5-diHE-oxathio
4-F-2-nHept-Ph
1-1005
3-HE-cPent
4-F-2-nHept-Ph
1-1006
4-HE-dioxo
4-F-2-nHept-Ph
1-1007
4-HE-dithio
4-F-2-nHept-Ph
1-1008
4-HE-oxathio
4-F-2-nHept-Ph
1-1009
3-HP-cPent
4-F-2-nHept-Ph
1-1010
4-HP-dioxo
4-F-2-nHept-Ph
1-1011
4-HP-dithio
4-F-2-nHept-Ph
1-1012
4-HP-oxathio
4-F-2-nHept-Ph
1-1013
3-HB-cPent
4-F-2-nHept-Ph
1-1014
4-HB-dioxo
4-F-2-nHept-Ph
1-1015
4-HB-dithio
4-F-2-nHept-Ph
1-1016
4-HB-oxathio
4-F-2-nHept-Ph
1-1017
ring 3
4-F-2-nHept-Ph
1-1018
ring 4
4-F-2-nHept-Ph
1-1019
ring 5
4-F-2-nHept-Ph
1-1020
ring 6
4-F-2-nHept-Ph
1-1021
ring 7
4-F-2-nHept-Ph
1-1022
ring 8
4-F-2-nHept-Ph
1-1023
ring 9
4-F-2-nHept-Ph
1-1024
ring 10
4-F-2-nHept-Ph
1-1025
3,4-diCH2NHAc-cPent
4-F-2-nHept-Ph
1-1026
4,5-diCH2NHAc-dioxo
4-F-2-nHept-Ph
1-1027
4,5-diCH2NHAc-dithio
4-F-2-nHept-Ph
1-1028
4,5-diCH2NHAc-oxathio
4-F-2-nHept-Ph
1-1029
ring 11
4-F-2-nHept-Ph
1-1030
ring 12
4-F-2-nHept-Ph
1-1031
ring 13
4-F-2-nHept-Ph
1-1032
ring 14
4-F-2-nHept-Ph
1-1033
4-OH-cHex
4-F-2-nHept-Ph
1-1034
5-OH-dioxa
4-F-2-nHept-Ph
1-1035
5-OH-dithia
4-F-2-nHept-Ph
1-1036
5-OH-oxathia
4-F-2-nHept-Ph
1-1037
4-NHAc-cHex
4-F-2-nHept-Ph
1-1038
5-NHAc-dioxa
4-F-2-nHept-Ph
1-1039
5-NHAc-dithia
4-F-2-nHept-Ph
1-1040
5-NHAc-oxathia
4-F-2-nHept-Ph
1-1041
4,4-diMe-cHex
4-F-2-nHept-Ph
1-1042
5,5-diMe-dioxa
4-F-2-nHept-Ph
1-1043
5,5-diMe-dithia
4-F-2-nHept-Ph
1-1044
5,5-diMe-oxathia
4-F-2-nHept-Ph
1-1045
4,4-diHM-cHex
4-F-2-nHept-Ph
1-1046
5,5-diHM-dioxa
4-F-2-nHept-Ph
1-1047
5,5-diHM-dithia
4-F-2-nHept-Ph
1-1048
5,5-diHM-oxathia
4-F-2-nHept-Ph
1-1049
ring 15
4-F-2-nHept-Ph
1-1050
ring 16
4-F-2-nHept-Ph
1-1051
ring 17
4-F-2-nHept-Ph
1-1052
ring 18
4-F-2-nHept-Ph
1-1053
4,4-diCO2Et-cHex
4-F-2-nHept-Ph
1-1054
5,5-diCO2Et-dioxa
4-F-2-nHept-Ph
1-1055
5,5-diCO2Et-dithia
4-F-2-nHept-Ph
1-1056
5,5-diCO2Et-oxathia
4-F-2-nHept-Ph
1-1057
H,H
Pyr
1-1058
O═
Pyr
1-1059
S═
Pyr
1-1060
cPent
Pyr
1-1061
cHex
Pyr
1-1062
dioxo
Pyr
1-1063
dioxa
Pyr
1-1064
dithio
Pyr
1-1065
dithia
Pyr
1-1066
oxathio
Pyr
1-1067
oxathia
Pyr
1-1068
4-HM-dioxo
Pyr
1-1069
4,5-diHM-dioxo
Pyr
1-1070
4,5-diHE-dioxo
Pyr
1-1071
5-OH-dioxa
Pyr
1-1072
5-NHAc-dioxa
Pyr
1-1073
5,5-diHM-dioxa
Pyr
1-1074
H,H
2-F—Pyr
1-1075
O═
2-F—Pyr
1-1076
S═
2-F—Pyr
1-1077
cPent
2-F—Pyr
1-1078
cHex
2-F—Pyr
1-1079
dioxo
2-F—Pyr
1-1080
dioxa
2-F—Pyr
1-1081
dithio
2-F—Pyr
1-1082
dithia
2-F—Pyr
1-1083
oxathia
2-F—Pyr
1-1084
oxathia
2-F—Pyr
1-1085
4-HM-dioxo
2-F—Pyr
1-1086
4,5-diHM-dioxo
2-F—Pyr
1-1087
4,5-diHE-dioxo
2-F—Pyr
1-1088
5-OH-dioxa
2-F—Pyr
1-1089
5-NHAc-dioxa
2-F—Pyr
1-1090
5,5-diHM-dioxa
2-F—Pyr
1-1091
H,H
2-Cl—Pyr
1-1092
O═
2-Cl—Pyr
1-1093
S═
2-Cl—Pyr
1-1094
cPent
2-Cl—Pyr
1-1095
cHex
2-Cl—Pyr
1-1096
dioxo
2-Cl—Pyr
1-1097
dioxa
2-Cl—Pyr
1-1098
dithio
2-Cl—Pyr
1-1099
dithia
2-Cl—Pyr
1-1100
oxathio
2-Cl—Pyr
1-1101
oxathia
2-Cl—Pyr
1-1102
4-HM-dioxo
2-Cl—Pyr
1-1103
4,5-diHM-dioxo
2-Cl—Pyr
1-1104
4,5-diHE-dioxo
2-Cl—Pyr
1-1105
5-OH-dioxa
2-Cl—Pyr
1-1106
5-NHAc-dioxa
2-Cl—Pyr
1-1107
5,5-diHM-dioxa
2-Cl—Pyr
1-1108
H,H
2-Br—Pyr
1-1109
O═
2-Br—Pyr
1-1110
S═
2-Br—Pyr
1-1111
cPent
2-Br—Pyr
1-1112
cHex
2-Br—Pyr
1-1113
dioxo
2-Br—Pyr
1-1114
dioxa
2-Br—Pyr
1-1115
dithio
2-Br—Pyr
1-1116
dithia
2-Br—Pyr
1-1117
oxathio
2-Br—Pyr
1-1118
oxathia
2-Br—Pyr
1-1119
4-HM-dioxo
2-Br—Pyr
1-1120
4,5-diHM-dioxo
2-Br—Pyr
1-1121
4,5-diHE-dioxo
2-Br—Pyr
1-1122
5-OH-dioxa
2-Br—Pyr
1-1123
5-NHAc-dioxa
2-Br—Pyr
1-1124
5,5-diHM-dioxa
2-Br—Pyr
1-1125
H,H
2,5-diF—Pyr
1-1126
O═
2,5-diF—Pyr
1-1127
S═
2,5-diF—Pyr
1-1128
cPent
2,5-diF—Pyr
1-1129
cHex
2,5-diF—Pyr
1-1130
dioxo
2,5-diF—Pyr
1-1131
dioxa
2,5-diF—Pyr
1-1132
dithio
2,5-diF—Pyr
1-1133
dithia
2,5-diF—Pyr
1-1134
oxathio
2,5-diF—Pyr
1-1135
oxathia
2,5-diF—Pyr
1-1136
4-HM-dioxo
2,5-diF—Pyr
1-1137
4,5-diHM-dioxo
2,5-diF—Pyr
1-1138
4,5-diHE-dioxo
2,5-diF—Pyr
1-1139
5-OH-dioxa
2,5-diF—Pyr
1-1140
5-NHAc-dioxa
2,5-diF—Pyr
1-1141
5,5-diHM-dioxa
2,5-diF—Pyr
1-1142
H,H
2,5-diCl—Pyr
1-1143
O═
2,5-diCl—Pyr
1-1144
S═
2,5-diCl—Pyr
1-1145
cPent
2,5-diCl—Pyr
1-1146
cHex
2,5-diCl—Pyr
1-1147
dioxo
2,5-diCl—Pyr
1-1148
dioxa
2,5-diCl—Pyr
1-1149
dithio
2,5-diCl—Pyr
1-1150
dithia
2,5-diCl—Pyr
1-1151
oxathio
2,5-diCl—Pyr
1-1152
oxathia
2,5-diCl—Pyr
1-1153
4-HM-dioxo
2,5-diCl—Pyr
1-1154
4,5-diHM-dioxo
2,5-diCl—Pyr
1-1155
4,5-diHE-dioxo
2,5-diCl—Pyr
1-1156
5-OH-dioxa
2,5-diCl—Pyr
1-1157
5-NHAc-dioxa
2,5-diCl—Pyr
1-1158
5,5-diHM-dioxa
2,5-diCl—Pyr
1-1159
H,H
2,5-diBr—Pyr
1-1160
O═
2,5-diBr—Pyr
1-1161
S═
2,5-diBr—Pyr
1-1162
cPent
2,5-diBr—Pyr
1-1163
cHex
2,5-diBr—Pyr
1-1164
dioxo
2,5-diBr—Pyr
1-1165
dioxa
2,5-diBr—Pyr
1-1166
dithio
2,5-diBr—Pyr
1-1167
dithia
2,5-diBr—Pyr
1-1168
oxathio
2,5-diBr—Pyr
1-1169
oxathia
2,5-diBr—Pyr
1-1170
4-HM-dioxo
2,5-diBr—Pyr
1-1171
4,5-diHM-dioxo
2,5-diBr—Pyr
1-1172
4,5-diHE-dioxo
2,5-diBr—Pyr
1-1173
5-OH-dioxa
2,5-diBr—Pyr
1-1174
5-NHAc-dioxa
2,5-diBr—Pyr
1-1175
5,5-diHM-dioxa
2,5-diBr—Pyr
1-1176
H,H
2-Me—Pyr
1-1177
O═
2-Me—Pyr
1-1178
S═
2-Me—Pyr
1-1179
cPent
2-Me—Pyr
1-1180
cHex
2-Me—Pyr
1-1181
dioxo
2-Me—Pyr
1-1182
dioxa
2-Me—Pyr
1-1183
dithio
2-Me—Pyr
1-1184
dithia
2-Me—Pyr
1-1185
oxathio
2-Me—Pyr
1-1186
oxathia
2-Me—Pyr
1-1187
4-HM-dioxo
2-Me—Pyr
1-1188
4,5-diHM-dioxo
2-Me—Pyr
1-1189
4,5-diHE-dioxo
2-Me—Pyr
1-1190
5-OH-dioxa
2-Me—Pyr
1-1191
5-NHAc-dioxa
2-Me—Pyr
1-1192
5,5-diHM-dioxa
2-Me—Pyr
1-1193
H,H
2-Et—Pyr
1-1194
O═
2-Et—Pyr
1-1195
S═
2-Et—Pyr
1-1196
cPent
2-Et—Pyr
1-1197
cHex
2-Et—Pyr
1-1198
dioxo
2-Et—Pyr
1-1199
dioxa
2-Et—Pyr
1-1200
dithio
2-Et—Pyr
1-1201
dithia
2-Et—Pyr
1-1202
oxathio
2-Et—Pyr
1-1203
oxathia
2-Et—Pyr
1-1204
4-HM-dioxo
2-Et—Pyr
1-1205
4,5-diHM-dioxo
2-Et—Pyr
1-1206
4,5-diHE-dioxo
2-Et—Pyr
1-1207
5-OH-dioxa
2-Et—Pyr
1-1208
5-NHAc-dioxa
2-Et—Pyr
1-1209
5,5-diHM-dioxa
2-Et—Pyr
1-1210
H,H
2-nPr—Pyr
1-1211
O═
2-nPr—Pyr
1-1212
S═
2-nPr—Pyr
1-1213
cPent
2-nPr—Pyr
1-1214
cHex
2-nPr—Pyr
1-1215
dioxo
2-nPr—Pyr
1-1216
dioxa
2-nPr—Pyr
1-1217
dithio
2-nPr—Pyr
1-1218
dithia
2-nPr—Pyr
1-1219
oxathio
2-nPr—Pyr
1-1220
oxathia
2-nPr—Pyr
1-1221
4-HM-dioxo
2-nPr—Pyr
1-1222
4,5-diHM-dioxo
2-nPr—Pyr
1-1223
4,5-diHE-dioxo
2-nPr—Pyr
1-1224
5-OH-dioxa
2-nPr—Pyr
1-1225
5-NHAc-dioxa
2-nPr—Pyr
1-1226
5,5-diHM-dioxa
2-nPr—Pyr
1-1227
H,H
2-nBu—Pyr
1-1228
O═
2-nBu—Pyr
1-1229
S═
2-nBu—Pyr
1-1230
cPent
2-nBu—Pyr
1-1231
cHex
2-nBu—Pyr
1-1232
dioxo
2-nBu—Pyr
1-1233
dioxa
2-nBu—Pyr
1-1234
dithio
2-nBu—Pyr
1-1235
dithia
2-nBu—Pyr
1-1236
oxathio
2-nBu—Pyr
1-1237
oxathia
2-nBu—Pyr
1-1238
4-HM-dioxo
2-nBu—Pyr
1-1239
4,5-diHM-dioxo
2-nBu—Pyr
1-1240
4,5-diHE-dioxo
2-nBu—Pyr
1-1241
5-OH-dioxa
2-nBu—Pyr
1-1242
5-NHAc-dioxa
2-nBu—Pyr
1-1243
5,5-diHM-dioxa
2-nBu—Pyr
1-1244
H,H
2-nPent-Pyr
1-1245
O═
2-nPent-Pyr
1-1246
S═
2-nPent-Pyr
1-1247
cPent
2-nPent-Pyr
1-1248
cHex
2-nPent-Pyr
1-1249
dioxo
2-nPent-Pyr
1-1250
dioxa
2-nPent-Pyr
1-1251
dithio
2-nPent-Pyr
1-1252
dithia
2-nPent-Pyr
1-1253
oxathio
2-nPent-Pyr
1-1254
oxathia
2-nPent-Pyr
1-1255
4-HM-dioxo
2-nPent-Pyr
1-1256
4,5-diHM-dioxo
2-nPent-Pyr
1-1257
4,5-diHE-dioxo
2-nPent-Pyr
1-1258
5-OH-dioxa
2-nPent-Pyr
1-1259
5-NHAc-dioxa
2-nPent-Pyr
1-1260
5,5-diHM-dioxa
2-nPent-Pyr
1-1261
H,H
2-nHex—Pyr
1-1262
O═
2-nHex—Pyr
1-1263
S═
2-nHex—Pyr
1-1264
cPent
2-nHex—Pyr
1-1265
cHex
2-nHex—Pyr
1-1266
dioxo
2-nHex—Pyr
1-1267
dioxa
2-nHex—Pyr
1-1268
dithio
2-nHex—Pyr
1-1269
dithia
2-nHex—Pyr
1-1270
oxathio
2-nHex—Pyr
1-1271
oxathia
2-nHex—Pyr
1-1272
4-HM-dioxo
2-nHex—Pyr
1-1273
4,5-diHM-dioxo
2-nHex—Pyr
1-1274
4,5-diHE-dioxo
2-nHex—Pyr
1-1275
5-OH-dioxa
2-nHex—Pyr
1-1276
5-NHAc-dioxa
2-nHex—Pyr
1-1277
5,5-diHM-dioxa
2-nHex—Pyr
1-1278
H,H
2-nHept-Pyr
1-1279
O═
2-nHept-Pyr
1-1280
S═
2-nHept-Pyr
1-1281
cPent
2-nHept-Pyr
1-1282
cHex
2-nHept-Pyr
1-1283
dioxo
2-nHept-Pyr
1-1284
dioxa
2-nHept-Pyr
1-1285
dithio
2-nHept-Pyr
1-1286
dithia
2-nHept-Pyr
1-1287
oxathio
2-nHept-Pyr
1-1288
oxathia
2-nHept-Pyr
1-1289
4-HM-dioxo
2-nHept-Pyr
1-1290
4,5-diHM-dioxo
2-nHept-Pyr
1-1291
4,5-diHE-dioxo
2-nHept-Pyr
1-1292
5-OH-dioxa
2-nHept-Pyr
1-1293
5-NHAc-dioxa
2-nHept-Pyr
1-1294
5,5-diHM-dioxa
2-nHept-Pyr
1-1295
H,H
2-nOct-Pyr
1-1296
O═
2-nOct-Pyr
1-1297
S═
2-nOct-Pyr
1-1298
cPent
2-nOct-Pyr
1-1299
cHex
2-nOct-Pyr
1-1300
dioxo
2-nOct-Pyr
1-1301
dioxa
2-nOct-Pyr
1-1302
dithio
2-nOct-Pyr
1-1303
dithia
2-nOct-Pyr
1-1304
oxathio
2-nOct-Pyr
1-1305
oxathia
2-nOct-Pyr
1-1306
4-HM-dioxo
2-nOct-Pyr
1-1307
4,5-diHM-dioxo
2-nOct-Pyr
1-1308
4,5-diHE-dioxo
2-nOct-Pyr
1-1309
5-OH-dioxa
2-nOct-Pyr
1-1310
5-NHAc-dioxa
2-nOct-Pyr
1-1311
5,5-diHM-dioxa
2-nOct-Pyr
1-1312
H,H
2-cPrl-Pyr
1-1313
O═
2-cPrl-Pyr
1-1314
S═
2-cPrl-Pyr
1-1315
cPent
2-cPrl-Pyr
1-1316
cHex
2-cPrl-Pyr
1-1317
dioxo
2-cPrl-Pyr
1-1318
dioxa
2-cPrl-Pyr
1-1319
dithio
2-cPrl-Pyr
1-1320
dithia
2-cPrl-Pyr
1-1321
oxathio
2-cPrl-Pyr
1-1322
oxathia
2-cPrl-Pyr
1-1323
4-HM-dioxo
2-cPrl-Pyr
1-1324
4,5-diHM-dioxo
2-cPrl-Pyr
1-1325
4,5-diHE-dioxo
2-cPrl-Pyr
1-1326
5-OH-dioxa
2-cPrl-Pyr
1-1327
5-NHAc-dioxa
2-cPrl-Pyr
1-1328
5,5-diHM-dioxa
2-cPrl-Pyr
1-1329
H,H
2-Ph—Pyr
1-1330
O═
2-Ph—Pyr
1-1331
S═
2-Ph—Pyr
1-1332
cPent
2-Ph—Pyr
1-1333
cHex
2-Ph—Pyr
1-1334
dioxo
2-Ph—Pyr
1-1335
dioxa
2-Ph—Pyr
1-1336
dithio
2-Ph—Pyr
1-1337
dithia
2-Ph—Pyr
1-1338
oxathio
2-Ph—Pyr
1-1339
oxathia
2-Ph—Pyr
1-1340
4-HM-dioxo
2-Ph—Pyr
1-1341
4,5-diHM-dioxo
2-Ph—Pyr
1-1342
4,5-diHE-dioxo
2-Ph—Pyr
1-1343
5-OH-dioxa
2-Ph—Pyr
1-1344
5-NHAc-dioxa
2-Ph—Pyr
1-1345
5,5-diHM-dioxa
2-Ph—Pyr
1-1346
H,H
2,5-diMe—Pyr
1-1347
O═
2,5-diMe—Pyr
1-1348
S═
2,5-diMe—Pyr
1-1349
cPent
2,5-diMe—Pyr
1-1350
cHex
2,5-diMe—Pyr
1-1351
dioxo
2,5-diMe—Pyr
1-1352
dioxa
2,5-diMe—Pyr
1-1353
dithio
2,5-diMe—Pyr
1-1354
dithia
2,5-diMe—Pyr
1-1355
oxathio
2,5-diMe—Pyr
1-1356
oxathia
2,5-diMe—Pyr
1-1357
4-HM-dioxo
2,5-diMe—Pyr
1-1358
4,5-diHM-dioxo
2,5-diMe—Pyr
1-1359
4,5-diHE-dioxo
2,5-diMe—Pyr
1-1360
5-OH-dioxa
2,5-diMe—Pyr
1-1361
5-NHAc-dioxa
2,5-diMe—Pyr
1-1362
5,5-diHM-dioxa
2,5-diMe—Pyr
1-1363
O═
2-Br—Ph
1-1364
S═
2-Br—Ph
1-1365
cPr
2-Br—Ph
1-1366
cBu
2-Br—Ph
1-1367
cPent
2-Br—Ph
1-1368
cHex
2-Br—Ph
1-1369
cHept
2-Br—Ph
1-1370
oxi
2-Br—Ph
1-1371
oxe
2-Br—Ph
1-1372
oxo
2-Br—Ph
1-1373
oxa
2-Br—Ph
1-1374
dioxo
2-Br—Ph
1-1375
dioxa
2-Br—Ph
1-1376
dioxe
2-Br—Ph
1-1377
dithio
2-Br—Ph
1-1378
dithia
2-Br—Ph
1-1379
ring 1
2-Br—Ph
1-1380
ring 2
2-Br—Ph
1-1381
oxathio
2-Br—Ph
1-1382
oxathia
2-Br—Ph
1-1383
ozl
2-Br—Ph
1-1384
ozn
2-Br—Ph
1-1385
tzl
2-Br—Ph
1-1386
tzn
2-Br—Ph
1-1387
3-HM-cPent
2-Br—Ph
1-1388
4-HM-dioxo
2-Br—Ph
1-1389
4-HM-dithio
2-Br—Ph
1-1390
4-HM-oxathio
2-Br—Ph
1-1391
3,4-diHM-cPent
2-Br—Ph
1-1392
4,5-diHM-dioxo
2-Br—Ph
1-1393
4,5-diHM-dithio
2-Br—Ph
1-1394
4,5-diHM-oxathio
2-Br—Ph
1-1395
3,4-diHE-cPent
2-Br—Ph
1-1396
4,5-diHE-dioxo
2-Br—Ph
1-1397
4,5-diHE-dithio
2-Br—Ph
1-1398
4,5-diHE-oxathio
2-Br—Ph
1-1399
3-HE-cPent
2-Br—Ph
1-1400
4-HE-dioxo
2-Br—Ph
1-1401
4-HE-dithio
2-Br—Ph
1-1402
4-HE-oxathio
2-Br—Ph
1-1403
3-HP-cPent
2-Br—Ph
1-1404
4-HP-dioxo
2-Br—Ph
1-1405
4-HP-dithio
2-Br—Ph
1-1406
4-HP-oxathio
2-Br—Ph
1-1407
3-HB-cPent
2-Br—Ph
1-1408
4-HB-dioxo
2-Br—Ph
1-1409
4-HB-dithio
2-Br—Ph
1-1410
4-HB-oxathio
2-Br—Ph
1-1411
ring 3
2-Br—Ph
1-1412
ring 4
2-Br—Ph
1-1413
ring 5
2-Br—Ph
1-1414
ring 6
2-Br—Ph
1-1415
ring 7
2-Br—Ph
1-1416
ring 8
2-Br—Ph
1-1417
ring 9
2-Br—Ph
1-1418
ring 10
2-Br—Ph
1-1419
3,4-diCH2NHAc-cPent
2-Br—Ph
1-1420
4,5-diCH2NHAc-dioxo
2-Br—Ph
1-1421
4,5-diCH2NHAc-dithio
2-Br—Ph
1-1422
4,5-diCH2NHAc-oxathio
2-Br—Ph
1-1423
ring 11
2-Br—Ph
1-1424
ring 12
2-Br—Ph
1-1425
ring 13
2-Br—Ph
1-1426
ring 14
2-Br—Ph
1-1427
4-OH-cHex
2-Br—Ph
1-1428
5-OH-dioxa
2-Br—Ph
1-1429
5-OH-dithia
2-Br—Ph
1-1430
5-OH-oxathia
2-Br—Ph
1-1431
4-NHAc-cHex
2-Br—Ph
1-1432
5-NHAc-dioxa
2-Br—Ph
1-1433
5-NHAc-dithia
2-Br—Ph
1-1434
5-NHAc-oxathia
2-Br—Ph
1-1435
4,4-diMe-cHex
2-Br—Ph
1-1436
5,5-diMe-dioxa
2-Br—Ph
1-1437
5,5-diMe-dithia
2-Br—Ph
1-1438
5,5-diMe-oxathia
2-Br—Ph
1-1439
4,4-diHM-cHex
2-Br—Ph
1-1440
5,5-diHM-dioxa
2-Br—Ph
1-1441
5,5-diHM-dithia
2-Br—Ph
1-1442
5,5-diHM-oxathia
2-Br—Ph
1-1443
ring 15
2-Br—Ph
1-1444
ring 16
2-Br—Ph
1-1445
ring 17
2-Br—Ph
1-1446
ring 18
2-Br—Ph
1-1447
4,4-diCO2Et-cHex
2-Br—Ph
1-1448
5,5-diCO2Et-dioxa
2-Br—Ph
1-1449
5,5-diCO2Et-dithia
2-Br—Ph
1-1450
5,5-diCO2Et-oxathia
2-Br—Ph
1-1451
O═
2-Cl-6-Me—Ph
1-1452
S═
2-Cl-6-Me—Ph
1-1453
cPr
2-Cl-6-Me—Ph
1-1454
cBu
2-Cl-6-Me—Ph
1-1455
cPent
2-Cl-6-Me—Ph
1-1456
cHex
2-Cl-6-Me—Ph
1-1457
cHept
2-Cl-6-Me—Ph
1-1458
oxi
2-Cl-6-Me—Ph
1-1459
oxe
2-Cl-6-Me—Ph
1-1460
oxo
2-Cl-6-Me—Ph
1-1461
oxa
2-Cl-6-Me—Ph
1-1462
dioxo
2-Cl-6-Me—Ph
1-1463
dioxa
2-Cl-6-Me—Ph
1-1464
dioxe
2-Cl-6-Me—Ph
1-1465
dithio
2-Cl-6-Me—Ph
1-1466
dithia
2-Cl-6-Me—Ph
1-1467
ring 1
2-Cl-6-Me—Ph
1-1468
ring 2
2-Cl-6-Me—Ph
1-1469
oxathio
2-Cl-6-Me—Ph
1-1470
oxathia
2-Cl-6-Me—Ph
1-1471
ozl
2-Cl-6-Me—Ph
1-1472
ozn
2-Cl-6-Me—Ph
1-1473
tzl
2-Cl-6-Me—Ph
1-1474
tzn
2-Cl-6-Me—Ph
1-1475
3-HM-cPent
2-Cl-6-Me—Ph
1-1476
4-HM-dioxo
2-Cl-6-Me—Ph
1-1477
4-HM-dithio
2-Cl-6-Me—Ph
1-1478
4-HM-oxathio
2-Cl-6-Me—Ph
1-1479
3,4-diHM-cPent
2-Cl-6-Me—Ph
1-1480
4,5-diHM-dioxo
2-Cl-6-Me—Ph
1-1481
4,5-diHM-dithio
2-Cl-6-Me—Ph
1-1482
4,5-diHM-oxathio
2-Cl-6-Me—Ph
1-1483
3,4-diHE-cPent
2-Cl-6-Me—Ph
1-1484
4,5-diHE-dioxo
2-Cl-6-Me—Ph
1-1485
4,5-diHE-dithio
2-Cl-6-Me—Ph
1-1486
4,5-diHE-oxathio
2-Cl-6-Me—Ph
1-1487
3-HE-cPent
2-Cl-6-Me—Ph
1-1488
4-HE-dioxo
2-Cl-6-Me—Ph
1-1489
4-HE-dithio
2-Cl-6-Me—Ph
1-1490
4-HE-oxathio
2-Cl-6-Me—Ph
1-1491
3-HP-cPent
2-Cl-6-Me—Ph
1-1492
4-HP-dioxo
2-Cl-6-Me—Ph
1-1493
4-HP-dithio
2-Cl-6-Me—Ph
1-1494
4-HP-oxathio
2-Cl-6-Me—Ph
1-1495
3-HB-cPent
2-Cl-6-Me—Ph
1-1496
4-HB-dioxo
2-Cl-6-Me—Ph
1-1497
4-HB-dithio
2-Cl-6-Me—Ph
1-1498
4-HB-oxathio
2-Cl-6-Me—Ph
1-1499
ring 3
2-Cl-6-Me—Ph
1-1500
ring 4
2-Cl-6-Me—Ph
1-1501
ring 5
2-Cl-6-Me—Ph
1-1502
ring 6
2-Cl-6-Me—Ph
1-1503
ring 7
2-Cl-6-Me—Ph
1-1504
ring 8
2-Cl-6-Me—Ph
1-1505
ring 9
2-Cl-6-Me—Ph
1-1506
ring 10
2-Cl-6-Me—Ph
1-1507
3,4-diCH2NHAc-cPent
2-Cl-6-Me—Ph
1-1508
4,5-diCH2NHAc-dioxo
2-Cl-6-Me—Ph
1-1509
4,5-diCH2NHAc-dithio
2-Cl-6-Me—Ph
1-1510
4,5-diCH2NHAc-oxathio
2-Cl-6-Me—Ph
1-1511
ring 11
2-Cl-6-Me—Ph
1-1512
ring 12
2-Cl-6-Me—Ph
1-1513
ring 13
2-Cl-6-Me—Ph
1-1514
ring 14
2-Cl-6-Me—Ph
1-1515
4-OH-cHex
2-Cl-6-Me—Ph
1-1516
5-OH-dioxa
2-Cl-6-Me—Ph
1-1517
5-OH-dithia
2-Cl-6-Me—Ph
1-1518
5-OH-oxathia
2-Cl-6-Me—Ph
1-1519
4-NHAc-cHex
2-Cl-6-Me—Ph
1-1520
5-NHAc-dioxa
2-Cl-6-Me—Ph
1-1521
5-NHAc-dithia
2-Cl-6-Me—Ph
1-1522
5-NHAc-oxathia
2-Cl-6-Me—Ph
1-1523
4,4-diMe-cHex
2-Cl-6-Me—Ph
1-1524
5,5-diMe-dioxa
2-Cl-6-Me—Ph
1-1525
5,5-diMe-dithia
2-Cl-6-Me—Ph
1-1526
5,5-diMe-oxathia
2-Cl-6-Me—Ph
1-1527
4,4-diHM-cHex
2-Cl-6-Me—Ph
1-1528
5,5-diHM-dioxa
2-Cl-6-Me—Ph
1-1529
5,5-diHM-dithia
2-Cl-6-Me—Ph
1-1530
5,5-diHM-oxathia
2-Cl-6-Me—Ph
1-1531
ring 15
2-Cl-6-Me—Ph
1-1532
ring 16
2-Cl-6-Me—Ph
1-1533
ring 17
2-Cl-6-Me—Ph
1-1534
ring 18
2-Cl-6-Me—Ph
1-1535
4,4-diCO2Et-cHex
2-Cl-6-Me—Ph
1-1536
5,5-diCO2Et-dioxa
2-Cl-6-Me—Ph
1-1537
5,5-diCO2Et-dithia
2-Cl-6-Me—Ph
1-1538
5,5-diCO2Et-oxathia
2-Cl-6-Me—Ph
1-1539
O═
2-Br-4-F—Ph
1-1540
S═
2-Br-4-F—Ph
1-1541
cPr
2-Br-4-F—Ph
1-1542
cBu
2-Br-4-F—Ph
1-1543
cPent
2-Br-4-F—Ph
1-1544
cHex
2-Br-4-F—Ph
1-1545
cHept
2-Br-4-F—Ph
1-1546
oxi
2-Br-4-F—Ph
1-1547
oxe
2-Br-4-F—Ph
1-1548
oxo
2-Br-4-F—Ph
1-1549
oxa
2-Br-4-F—Ph
1-1550
dioxo
2-Br-4-F—Ph
1-1551
dioxa
2-Br-4-F—Ph
1-1552
dioxe
2-Br-4-F—Ph
1-1553
dithio
2-Br-4-F—Ph
1-1554
dithia
2-Br-4-F—Ph
1-1555
ring 1
2-Br-4-F—Ph
1-1556
ring 2
2-Br-4-F—Ph
1-1557
oxathio
2-Br-4-F—Ph
1-1558
oxathia
2-Br-4-F—Ph
1-1559
ozl
2-Br-4-F—Ph
1-1560
ozn
2-Br-4-F—Ph
1-1561
tzl
2-Br-4-F—Ph
1-1562
tzn
2-Br-4-F—Ph
1-1563
3-HM-cPent
2-Br-4-F—Ph
1-1564
4-HM-dioxo
2-Br-4-F—Ph
1-1565
4-HM-dithio
2-Br-4-F—Ph
1-1566
4-HM-oxathio
2-Br-4-F—Ph
1-1567
3,4-diHM-cPent
2-Br-4-F—Ph
1-1568
4,5-diHM-dioxo
2-Br-4-F—Ph
1-1569
4,5-diHM-dithio
2-Br-4-F—Ph
1-1570
4,5-diHM-oxathio
2-Br-4-F—Ph
1-1571
3,4-diHE-cPent
2-Br-4-F—Ph
1-1572
4,5-diHE-dioxo
2-Br-4-F—Ph
1-1573
4,5-diHE-dithio
2-Br-4-F—Ph
1-1574
4,5-diHE-oxathio
2-Br-4-F—Ph
1-1575
3-HE-cPent
2-Br-4-F—Ph
1-1576
4-HE-dioxo
2-Br-4-F—Ph
1-1577
4-HE-dithio
2-Br-4-F—Ph
1-1578
4-HE-oxathio
2-Br-4-F—Ph
1-1579
3-HP-cPent
2-Br-4-F—Ph
1-1580
4-HP-dioxo
2-Br-4-F—Ph
1-1581
4-HP-dithio
2-Br-4-F—Ph
1-1582
4-HP-oxathio
2-Br-4-F—Ph
1-1583
3-HB-cPent
2-Br-4-F—Ph
1-1584
4-HB-dioxo
2-Br-4-F—Ph
1-1585
4-HB-dithio
2-Br-4-F—Ph
1-1586
4-HB-oxathio
2-Br-4-F—Ph
1-1587
ring 3
2-Br-4-F—Ph
1-1588
ring 4
2-Br-4-F—Ph
1-1589
ring 5
2-Br-4-F—Ph
1-1590
ring 6
2-Br-4-F—Ph
1-1591
ring 7
2-Br-4-F—Ph
1-1592
ring 8
2-Br-4-F—Ph
1-1593
ring 9
2-Br-4-F—Ph
1-1594
ring 10
2-Br-4-F—Ph
1-1595
3,4-diCH2NHAc-cPent
2-Br-4-F—Ph
1-1596
4,5-diCH2NHAc-dioxo
2-Br-4-F—Ph
1-1597
4,5-diCH2NHAc-dithio
2-Br-4-F—Ph
1-1598
4,5-diCH2NHAc-oxathio
2-Br-4-F—Ph
1-1599
ring 11
2-Br-4-F—Ph
1-1600
ring 12
2-Br-4-F—Ph
1-1601
ring 13
2-Br-4-F—Ph
1-1602
ring 14
2-Br-4-F—Ph
1-1603
4-OH-cHex
2-Br-4-F—Ph
1-1604
5-OH-dioxa
2-Br-4-F—Ph
1-1605
5-OH-dithia
2-Br-4-F—Ph
1-1606
5-OH-oxathia
2-Br-4-F—Ph
1-1607
4-NHAc-cHex
2-Br-4-F—Ph
1-1608
5-NHAc-dioxa
2-Br-4-F—Ph
1-1609
5-NHAc-dithia
2-Br-4-F—Ph
1-1610
5-NHAc-oxathia
2-Br-4-F—Ph
1-1611
4,4-diMe-cHex
2-Br-4-F—Ph
1-1612
5,5-diMe-dioxa
2-Br-4-F—Ph
1-1613
5,5-diMe-dithia
2-Br-4-F—Ph
1-1614
5,5-diMe-oxathia
2-Br-4-F—Ph
1-1615
4,4-diHM-cHex
2-Br-4-F—Ph
1-1616
5,5-diHM-dioxa
2-Br-4-F—Ph
1-1617
5,5-diHM-dithia
2-Br-4-F—Ph
1-1618
5,5-diHM-oxathia
2-Br-4-F—Ph
1-1619
ring 15
2-Br-4-F—Ph
1-1620
ring 16
2-Br-4-F—Ph
1-1621
ring 17
2-Br-4-F—Ph
1-1622
ring 18
2-Br-4-F—Ph
1-1623
4,4-diCO2Et-cHex
2-Br-4-F—Ph
1-1624
5,5-diCO2Et-dioxa
2-Br-4-F—Ph
1-1625
5,5-diCO2Et-dithia
2-Br-4-F—Ph
1-1626
5,5-diCO2Et-oxathia
2-Br-4-F—Ph
1-1627
O═
2-nPent-Ph
1-1628
S═
2-nPent-Ph
1-1629
cPr
2-nPent-Ph
1-1630
cBu
2-nPent-Ph
1-1631
cPent
2-nPent-Ph
1-1632
cHex
2-nPent-Ph
1-1633
cHept
2-nPent-Ph
1-1634
oxi
2-nPent-Ph
1-1635
oxe
2-nPent-Ph
1-1636
oxo
2-nPent-Ph
1-1637
oxa
2-nPent-Ph
1-1638
dioxo
2-nPent-Ph
1-1639
dioxa
2-nPent-Ph
1-1640
dioxe
2-nPent-Ph
1-1641
dithio
2-nPent-Ph
1-1642
dithia
2-nPent-Ph
1-1643
ring 1
2-nPent-Ph
1-1644
ring 2
2-nPent-Ph
1-1645
oxathio
2-nPent-Ph
1-1646
oxathia
2-nPent-Ph
1-1647
ozl
2-nPent-Ph
1-1648
ozn
2-nPent-Ph
1-1649
tzl
2-nPent-Ph
1-1650
tzn
2-nPent-Ph
1-1651
3-HM-cPent
2-nPent-Ph
1-1652
4-HM-dioxo
2-nPent-Ph
1-1653
4-HM-dithio
2-nPent-Ph
1-1654
4-HM-oxathio
2-nPent-Ph
1-1655
3,4-diHM-cPent
2-nPent-Ph
1-1656
4,5-diHM-dioxo
2-nPent-Ph
1-1657
4,5-diHM-dithio
2-nPent-Ph
1-1658
4,5-diHM-oxathio
2-nPent-Ph
1-1659
3,4-diHE-cPent
2-nPent-Ph
1-1660
4,5-diHE-dioxo
2-nPent-Ph
1-1661
4,5-diHE-dithio
2-nPent-Ph
1-1662
4,5-diHE-oxathio
2-nPent-Ph
1-1663
3-HE-cPent
2-nPent-Ph
1-1664
4-HE-dioxo
2-nPent-Ph
1-1665
4-HE-dithio
2-nPent-Ph
1-1666
4-HE-oxathio
2-nPent-Ph
1-1667
3-HP-cPent
2-nPent-Ph
1-1668
4-HP-dioxo
2-nPent-Ph
1-1669
4-HP-dithio
2-nPent-Ph
1-1670
4-HP-oxathio
2-nPent-Ph
1-1671
3-HB-cPent
2-nPent-Ph
1-1672
4-HB-dioxo
2-nPent-Ph
1-1673
4-HB-dithio
2-nPent-Ph
1-1674
4-HB-oxathio
2-nPent-Ph
1-1675
ring 3
2-nPent-Ph
1-1676
ring 4
2-nPent-Ph
1-1677
ring 5
2-nPent-Ph
1-1678
ring 6
2-nPent-Ph
1-1679
ring 7
2-nPent-Ph
1-1680
ring 8
2-nPent-Ph
1-1681
ring 9
2-nPent-Ph
1-1682
ring 10
2-nPent-Ph
1-1683
3,4-diCH2NHAc-cPent
2-nPent-Ph
1-1684
4,5-diCH2NHAc-dioxo
2-nPent-Ph
1-1685
4,5-diCH2NHAc-dithio
2-nPent-Ph
1-1686
4,5-diCH2NHAc-oxathio
2-nPent-Ph
1-1687
ring 11
2-nPent-Ph
1-1688
ring 12
2-nPent-Ph
1-1689
ring 13
2-nPent-Ph
1-1690
ring 14
2-nPent-Ph
1-1691
4-OH-cHex
2-nPent-Ph
1-1692
5-OH-dioxa
2-nPent-Ph
1-1693
5-OH-dithia
2-nPent-Ph
1-1694
5-OH-oxathia
2-nPent-Ph
1-1695
4-NHAc-cHex
2-nPent-Ph
1-1696
5-NHAc-dioxa
2-nPent-Ph
1-1697
5-NHAc-dithia
2-nPent-Ph
1-1698
5-NHAc-oxathia
2-nPent-Ph
1-1699
4,4-diMe-cHex
2-nPent-Ph
1-1700
5,5-diMe-dioxa
2-nPent-Ph
1-1701
5,5-diMe-dithia
2-nPent-Ph
1-1702
5,5-diMe-oxathia
2-nPent-Ph
1-1703
4,4-diHM-cHex
2-nPent-Ph
1-1704
5,5-diHM-dioxa
2-nPent-Ph
1-1705
5,5-diHM-dithia
2-nPent-Ph
1-1706
5,5-diHM-oxathia
2-nPent-Ph
1-1707
ring 15
2-nPent-Ph
1-1708
ring 16
2-nPent-Ph
1-1709
ring 17
2-nPent-Ph
1-1710
ring 18
2-nPent-Ph
1-1711
4,4-diCO2Et-cHex
2-nPent-Ph
1-1712
5,5-diCO2Et-dioxa
2-nPent-Ph
1-1713
5,5-diCO2Et-dithia
2-nPent-Ph
1-1714
5,5-diCO2Et-oxathia
2-nPent-Ph
1-1715
O═
4-F-2-nPent-Ph
1-1716
S═
4-F-2-nPent-Ph
1-1717
cPr
4-F-2-nPent-Ph
1-1718
cBu
4-F-2-nPent-Ph
1-1719
cPent
4-F-2-nPent-Ph
1-1720
cHex
4-F-2-nPent-Ph
1-1721
cHept
4-F-2-nPent-Ph
1-1722
oxi
4-F-2-nPent-Ph
1-1723
oxe
4-F-2-nPent-Ph
1-1724
oxo
4-F-2-nPent-Ph
1-1725
oxa
4-F-2-nPent-Ph
1-1726
dioxo
4-F-2-nPent-Ph
1-1727
dioxa
4-F-2-nPent-Ph
1-1728
dioxe
4-F-2-nPent-Ph
1-1729
dithio
4-F-2-nPent-Ph
1-1730
dithia
4-F-2-nPent-Ph
1-1731
ring 1
4-F-2-nPent-Ph
1-1732
ring 2
4-F-2-nPent-Ph
1-1733
oxathio
4-F-2-nPent-Ph
1-1734
oxathia
4-F-2-nPent-Ph
1-1735
ozl
4-F-2-nPent-Ph
1-1736
ozn
4-F-2-nPent-Ph
1-1737
tzl
4-F-2-nPent-Ph
1-1738
tzn
4-F-2-nPent-Ph
1-1739
3-HM-cPent
4-F-2-nPent-Ph
1-1740
4-HM-dioxo
4-F-2-nPent-Ph
1-1741
4-HM-dithio
4-F-2-nPent-Ph
1-1742
4-HM-oxathio
4-F-2-nPent-Ph
1-1743
3,4-diHM-cPent
4-F-2-nPent-Ph
1-1744
4,5-diHM-dioxo
4-F-2-nPent-Ph
1-1745
4,5-diHM-dithio
4-F-2-nPent-Ph
1-1746
4,5-diHM-oxathio
4-F-2-nPent-Ph
1-1747
3,4-diHE-cPent
4-F-2-nPent-Ph
1-1748
4,5-diHE-dioxo
4-F-2-nPent-Ph
1-1749
4,5-diHE-dithio
4-F-2-nPent-Ph
1-1750
4,5-diHE-oxathio
4-F-2-nPent-Ph
1-1751
3-HE-cPent
4-F-2-nPent-Ph
1-1752
4-HE-dioxo
4-F-2-nPent-Ph
1-1753
4-HE-dithio
4-F-2-nPent-Ph
1-1754
4-HE-oxathio
4-F-2-nPent-Ph
1-1755
3-HP-cPent
4-F-2-nPent-Ph
1-1756
4-HP-dioxo
4-F-2-nPent-Ph
1-1757
4-HP-dithio
4-F-2-nPent-Ph
1-1758
4-HP-oxathio
4-F-2-nPent-Ph
1-1759
3-HB-cPent
4-F-2-nPent-Ph
1-1760
4-HB-dioxo
4-F-2-nPent-Ph
1-1761
4-HB-dithio
4-F-2-nPent-Ph
1-1762
4-HB-oxathio
4-F-2-nPent-Ph
1-1763
ring 3
4-F-2-nPent-Ph
1-1764
ring 4
4-F-2-nPent-Ph
1-1765
ring 5
4-F-2-nPent-Ph
1-1766
ring 6
4-F-2-nPent-Ph
1-1767
ring 7
4-F-2-nPent-Ph
1-1768
ring 8
4-F-2-nPent-Ph
1-1769
ring 9
4-F-2-nPent-Ph
1-1770
ring 10
4-F-2-nPent-Ph
1-1771
3,4-diCH2NHAc-cPent
4-F-2-nPent-Ph
1-1772
4,5-diCH2NHAc-dioxo
4-F-2-nPent-Ph
1-1773
4,5-diCH2NHAc-dithio
4-F-2-nPent-Ph
1-1774
4,5-diCH2NHAc-oxathio
4-F-2-nPent-Ph
1-1775
ring 11
4-F-2-nPent-Ph
1-1776
ring 12
4-F-2-nPent-Ph
1-1777
ring 13
4-F-2-nPent-Ph
1-1778
ring 14
4-F-2-nPent-Ph
1-1779
4-OH-cHex
4-F-2-nPent-Ph
1-1780
5-OH-dioxa
4-F-2-nPent-Ph
1-1781
5-OH-dithia
4-F-2-nPent-Ph
1-1782
5-OH-oxathia
4-F-2-nPent-Ph
1-1783
4-NHAc-cHex
4-F-2-nPent-Ph
1-1784
5-NHAc-dioxa
4-F-2-nPent-Ph
1-1785
5-NHAc-dithia
4-F-2-nPent-Ph
1-1786
5-NHAc-oxathia
4-F-2-nPent-Ph
1-1787
4,4-diMe-cHex
4-F-2-nPent-Ph
1-1788
5,5-diMe-dioxa
4-F-2-nPent-Ph
1-1789
5,5-diMe-dithia
4-F-2-nPent-Ph
1-1790
5,5-diMe-oxathia
4-F-2-nPent-Ph
1-1791
4,4-diHM-cHex
4-F-2-nPent-Ph
1-1792
5,5-diHM-dioxa
4-F-2-nPent-Ph
1-1793
5,5-diHM-dithia
4-F-2-nPent-Ph
1-1794
5,5-diHM-oxathia
4-F-2-nPent-Ph
1-1795
ring 15
4-F-2-nPent-Ph
1-1796
ring 16
4-F-2-nPent-Ph
1-1797
ring 17
4-F-2-nPent-Ph
1-1798
ring 18
4-F-2-nPent-Ph
1-1799
4,4-diCO2Et-cHex
4-F-2-nPent-Ph
1-1800
5,5-diCO2Et-dioxa
4-F-2-nPent-Ph
1-1801
5,5-diCO2Et-dithia
4-F-2-nPent-Ph
1-1802
5,5-diCO2Et-oxathia
4-F-2-nPent-Ph
1-1803
O═
2-nOct-Ph
1-1804
S═
2-nOct-Ph
1-1805
cPr
2-nOct-Ph
1-1806
cBu
2-nOct-Ph
1-1807
cPent
2-nOct-Ph
1-1808
cHex
2-nOct-Ph
1-1809
cHept
2-nOct-Ph
1-1810
oxi
2-nOct-Ph
1-1811
oxe
2-nOct-Ph
1-1812
oxo
2-nOct-Ph
1-1813
oxa
2-nOct-Ph
1-1814
dioxo
2-nOct-Ph
1-1815
dioxa
2-nOct-Ph
1-1816
dioxe
2-nOct-Ph
1-1817
dithio
2-nOct-Ph
1-1818
dithia
2-nOct-Ph
1-1819
ring 1
2-nOct-Ph
1-1820
ring 2
2-nOct-Ph
1-1821
oxathio
2-nOct-Ph
1-1822
oxathia
2-nOct-Ph
1-1823
ozl
2-nOct-Ph
1-1824
ozn
2-nOct-Ph
1-1825
tzl
2-nOct-Ph
1-1826
tzn
2-nOct-Ph
1-1827
3-HM-cPent
2-nOct-Ph
1-1828
4-HM-dioxo
2-nOct-Ph
1-1829
4-HM-dithio
2-nOct-Ph
1-1830
4-HM-oxathio
2-nOct-Ph
1-1831
3,4-diHM-cPent
2-nOct-Ph
1-1832
4,5-diHM-dioxo
2-nOct-Ph
1-1833
4,5-diHM-dithio
2-nOct-Ph
1-1834
4,5-diHM-oxathio
2-nOct-Ph
1-1835
3,4-diHE-cPent
2-nOct-Ph
1-1836
4,5-diHE-dioxo
2-nOct-Ph
1-1837
4,5-diHE-dithio
2-nOct-Ph
1-1838
4,5-diHE-oxathio
2-nOct-Ph
1-1839
3-HE-cPent
2-nOct-Ph
1-1840
4-HE-dioxo
2-nOct-Ph
1-1841
4-HE-dithio
2-nOct-Ph
1-1842
4-HE-oxathio
2-nOct-Ph
1-1843
3-HP-cPent
2-nOct-Ph
1-1844
4-HP-dioxo
2-nOct-Ph
1-1845
4-HP-dithio
2-nOct-Ph
1-1846
4-HP-oxathio
2-nOct-Ph
1-1847
3-HB-cPent
2-nOct-Ph
1-1848
4-HB-dioxo
2-nOct-Ph
1-1849
4-HB-dithio
2-nOct-Ph
1-1850
4-HB-oxathio
2-nOct-Ph
1-1851
ring 3
2-nOct-Ph
1-1852
ring 4
2-nOct-Ph
1-1853
ring 5
2-nOct-Ph
1-1854
ring 6
2-nOct-Ph
1-1855
ring 7
2-nOct-Ph
1-1856
ring 8
2-nOct-Ph
1-1857
ring 9
2-nOct-Ph
1-1858
ring 10
2-nOct-Ph
1-1859
3,4-diCH2NHAc-cPent
2-nOct-Ph
1-1860
4,5-diCH2NHAc-dioxo
2-nOct-Ph
1-1861
4,5-diCH2NHAc-dithio
2-nOct-Ph
1-1862
4,5-diCH2NHAc-oxathio
2-nOct-Ph
1-1863
ring 11
2-nOct-Ph
1-1864
ring 12
2-nOct-Ph
1-1865
ring 13
2-nOct-Ph
1-1866
ring 14
2-nOct-Ph
1-1867
4-OH-cHex
2-nOct-Ph
1-1868
5-OH-dioxa
2-nOct-Ph
1-1869
5-OH-dithia
2-nOct-Ph
1-1870
5-OH-oxathia
2-nOct-Ph
1-1871
4-NHAc-cHex
2-nOct-Ph
1-1872
5-NHAc-dioxa
2-nOct-Ph
1-1873
5-NHAc-dithia
2-nOct-Ph
1-1874
5-NHAc-oxathia
2-nOct-Ph
1-1875
4,4-diMe-cHex
2-nOct-Ph
1-1876
5,5-diMe-dioxa
2-nOct-Ph
1-1877
5,5-diMe-dithia
2-nOct-Ph
1-1878
5,5-diMe-oxathia
2-nOct-Ph
1-1879
4,4-diHM-cHex
2-nOct-Ph
1-1880
5,5-diHM-dioxa
2-nOct-Ph
1-1881
5,5-diHM-dithia
2-nOct-Ph
1-1882
5,5-diHM-oxathia
2-nOct-Ph
1-1883
ring 15
2-nOct-Ph
1-1884
ring 16
2-nOct-Ph
1-1885
ring 17
2-nOct-Ph
1-1886
ring 18
2-nOct-Ph
1-1887
4,4-diCO2Et-cHex
2-nOct-Ph
1-1888
5,5-diCO2Et-dioxa
2-nOct-Ph
1-1889
5,5-diCO2Et-dithia
2-nOct-Ph
1-1890
5,5-diCO2Et-oxathia
2-nOct-Ph
1-1891
O═
4-F-2-nOct-Ph
1-1892
S═
4-F-2-nOct-Ph
1-1893
cPr
4-F-2-nOct-Ph
1-1894
cBu
4-F-2-nOct-Ph
1-1895
cPent
4-F-2-nOct-Ph
1-1896
cHex
4-F-2-nOct-Ph
1-1897
cHept
4-F-2-nOct-Ph
1-1898
oxi
4-F-2-nOct-Ph
1-1899
oxe
4-F-2-nOct-Ph
1-1900
oxo
4-F-2-nOct-Ph
1-1901
oxa
4-F-2-nOct-Ph
1-1902
diaxo
4-F-2-nOct-Ph
1-1903
dioxa
4-F-2-nOct-Ph
1-1904
dioxe
4-F-2-nOct-Ph
1-1905
dithio
4-F-2-nOct-Ph
1-1906
dithia
4-F-2-nOct-Ph
1-1907
ring 1
4-F-2-nOct-Ph
1-1908
ring 2
4-F-2-nOct-Ph
1-1909
oxathio
4-F-2-nOct-Ph
1-1910
oxathia
4-F-2-nOct-Ph
1-1911
ozl
4-F-2-nOct-Ph
1-1912
ozn
4-F-2-nOct-Ph
1-1913
tzl
4-F-2-nOct-Ph
1-1914
tzn
4-F-2-nOct-Ph
1-1915
3-HM-cPent
4-F-2-nOct-Ph
1-1916
4-HM-dioxo
4-F-2-nOct-Ph
1-1917
4-HM-dithio
4-F-2-nOct-Ph
1-1918
4-HM-oxathio
4-F-2-nOct-Ph
1-1919
3,4-diHM-cPent
4-F-2-nOct-Ph
1-1920
4,5-diHM-dioxo
4-F-2-nOct-Ph
1-1921
4,5-diHM-dithio
4-F-2-nOct-Ph
1-1922
4,5-diHM-oxathio
4-F-2-nOct-Ph
1-1923
3,4-diHE-cPent
4-F-2-nOct-Ph
1-1924
4,5-diHE-dioxo
4-F-2-nOct-Ph
1-1925
4,5-diHE-dithio
4-F-2-nOct-Ph
1-1926
4,5-diHE-oxathio
4-F-2-nOct-Ph
1-1927
3-HE-cPent
4-F-2-nOct-Ph
1-1928
4-HE-dioxo
4-F-2-nOct-Ph
1-1929
4-HE-dithio
4-F-2-nOct-Ph
1-1930
4-HE-oxathio
4-F-2-nOct-Ph
1-1931
3-HP-cPent
4-F-2-nOct-Ph
1-1932
4-HP-dioxo
4-F-2-nOct-Ph
1-1933
4-HP-dithio
4-F-2-nOct-Ph
1-1934
4-HP-oxathio
4-F-2-nOct-Ph
1-1935
3-HB-cPent
4-F-2-nOct-Ph
1-1936
4-HB-dioxo
4-F-2-nOct-Ph
1-1937
4-HB-dithio
4-F-2-nOct-Ph
1-1938
4-HB-oxathio
4-F-2-nOct-Ph
1-1939
ring 3
4-F-2-nOct-Ph
1-1940
ring 4
4-F-2-nOct-Ph
1-1941
ring 5
4-F-2-nOct-Ph
1-1942
ring 6
4-F-2-nOct-Ph
1-1943
ring 7
4-F-2-nOct-Ph
1-1944
ring 8
4-F-2-nOct-Ph
1-1945
ring 9
4-F-2-nOct-Ph
1-1946
ring 10
4-F-2-nOct-Ph
1-1947
3,4-diCH2NHAc-cPent
4-F-2-nOct-Ph
1-1948
4,5-diCH2NHAc-dioxo
4-F-2-nOct-Ph
1-1949
4,5-diCH2NHAc-dithio
4-F-2-nOct-Ph
1-1950
4,5-diCH2NHAc-oxathio
4-F-2-nOct-Ph
1-1951
ring 11
4-F-2-nOct-Ph
1-1952
ring 12
4-F-2-nOct-Ph
1-1953
ring 13
4-F-2-nOct-Ph
1-1954
ring 14
4-F-2-nOct-Ph
1-1955
4-OH-cHex
4-F-2-nOct-Ph
1-1956
5-OH-dioxa
4-F-2-nOct-Ph
1-1957
5-OH-dithia
4-F-2-nOct-Ph
1-1958
5-OH-oxathia
4-F-2-nOct-Ph
1-1959
4-NHAc-cHex
4-F-2-nOct-Ph
1-1960
5-NHAc-dioxa
4-F-2-nOct-Ph
1-1961
5-NHAc-dithia
4-F-2-nOct-Ph
1-1962
5-NHAc-oxathia
4-F-2-nOct-Ph
1-1963
4,4-diMe-cHex
4-F-2-nOct-Ph
1-1964
5,5-diMe-dioxa
4-F-2-nOct-Ph
1-1965
5,5-diMe-dithia
4-F-2-nOct-Ph
1-1966
5,5-diMe-oxathia
4-F-2-nOct-Ph
1-1967
4,4-diHM-cHex
4-F-2-nOct-Ph
1-1968
5,5-diHM-dioxa
4-F-2-nOct-Ph
1-1969
5,5-diHM-dithia
4-F-2-nOct-Ph
1-1970
5,5-diHM-oxathia
4-F-2-nOct-Ph
1-1971
ring 15
4-F-2-nOct-Ph
1-1972
ring 16
4-F-2-nOct-Ph
1-1973
ring 17
4-F-2-nOct-Ph
1-1974
ring 18
4-F-2-nOct-Ph
1-1975
4,4-diCO2Et-cHex
4-F-2-nOct-Ph
1-1976
5,5-diCO2Et-dioxa
4-F-2-nOct-Ph
1-1977
5,5-diCO2Et-dithia
4-F-2-nOct-Ph
1-1978
O═
2-nPr—Ph
1-1979
S═
2-nPr—Ph
1-1980
cPr
2-nPr—Ph
1-1981
cBu
2-nPr—Ph
1-1982
cPent
2-nPr—Ph
1-1983
cHex
2-nPr—Ph
1-1984
cHept
2-nPr—Ph
1-1985
oxi
2-nPr—Ph
1-1986
oxe
2-nPr—Ph
1-1987
oxo
2-nPr—Ph
1-1988
oxa
2-nPr—Ph
1-1989
dioxo
2-nPr—Ph
1-1990
dioxa
2-nPr—Ph
1-1991
dioxe
2-nPr—Ph
1-1992
dithio
2-nPr—Ph
1-1993
dithia
2-nPr—Ph
1-1994
ring 1
2-nPr—Ph
1-1995
ring 2
2-nPr—Ph
1-1996
oxathio
2-nPr—Ph
1-1997
oxathia
2-nPr—Ph
1-1998
ozl
2-nPr—Ph
1-1999
ozn
2-nPr—Ph
1-2000
tzl
2-nPr—Ph
1-2001
tzn
2-nPr—Ph
1-2002
3-HM-cPent
2-nPr—Ph
1-2003
4-HM-dioxo
2-nPr—Ph
1-2004
4-HM-dithio
2-nPr—Ph
1-2005
4-HM-oxathio
2-nPr—Ph
1-2006
3,4-diHM-cPent
2-nPr—Ph
1-2007
4,5-diHM-dioxo
2-nPr—Ph
1-2008
4,5-diHM-dithio
2-nPr—Ph
1-2009
4,5-diHM-oxathio
2-nPr—Ph
1-2010
3,4-diHE-cPent
2-nPr—Ph
1-2011
4,5-diHE-dioxo
2-nPr—Ph
1-2012
4,5-diHE-dithio
2-nPr—Ph
1-2013
4,5-diHE-oxathio
2-nPr—Ph
1-2014
3-HE-cPent
2-nPr—Ph
1-2015
4-HE-dioxo
2-nPr—Ph
1-2016
4-HE-dithio
2-nPr—Ph
1-2017
4-HE-oxathio
2-nPr—Ph
1-2018
3-HP-cPent
2-nPr—Ph
1-2019
4-HP-dioxo
2-nPr—Ph
1-2020
4-HP-dithio
2-nPr—Ph
1-2021
4-HP-oxathio
2-nPr—Ph
1-2022
3-HB-cPent
2-nPr—Ph
1-2023
4-HB-dioxo
2-nPr—Ph
1-2024
4-HB-dithio
2-nPr—Ph
1-2025
4-HB-oxathio
2-nPr—Ph
1-2026
ring 3
2-nPr—Ph
1-2027
ring 4
2-nPr—Ph
1-2028
ring 5
2-nPr—Ph
1-2029
ring 6
2-nPr—Ph
1-2030
ring 7
2-nPr—Ph
1-2031
ring 8
2-nPr—Ph
1-2032
ring 9
2-nPr—Ph
1-2033
ring 10
2-nPr—Ph
1-2034
3,4-diCH2NHAc-cPent
2-nPr—Ph
1-2035
4,5-diCH2NHAc-dioxo
2-nPr—Ph
1-2036
4,5-diCH2NHAc-dithio
2-nPr—Ph
1-2037
4,5-diCH2NHAc-oxathio
2-nPr—Ph
1-2038
ring 11
2-nPr—Ph
1-2039
ring 12
2-nPr—Ph
1-2040
ring 13
2-nPr—Ph
1-2041
ring 14
2-nPr—Ph
1-2042
4-OH-cHex
2-nPr—Ph
1-2043
5-OH-dioxa
2-nPr—Ph
1-2044
5-OH-dithia
2-nPr—Ph
1-2045
5-OH-oxathia
2-nPr—Ph
1-2046
4-NHAc-cHex
2-nPr—Ph
1-2047
5-NHAc-dioxa
2-nPr—Ph
1-2048
5-NHAc-dithia
2-nPr—Ph
1-2049
5-NHAc-oxathia
2-nPr—Ph
1-2050
4,4-diMe-cHex
2-nPr—Ph
1-2051
5,5-diMe-dioxa
2-nPr—Ph
1-2052
5,5-diMe-dithia
2-nPr—Ph
1-2053
5,5-diMe-oxathia
2-nPr—Ph
1-2054
4,4-diHM-cHex
2-nPr—Ph
1-2055
5,5-diHM-dioxa
2-nPr—Ph
1-2056
5,5-diHM-dithia
2-nPr—Ph
1-2057
5,5-diHM-oxathia
2-nPr—Ph
1-2058
ring 15
2-nPr—Ph
1-2059
ring 16
2-nPr—Ph
1-2060
ring 17
2-nPr—Ph
1-2061
ring 18
2-nPr—Ph
1-2062
4,4-diCO2Et-cHex
2-nPr—Ph
1-2063
5,5-diCO2Et-dioxa
2-nPr—Ph
1-2064
5,5-diCO2Et-dithia
2-nPr—Ph
1-2065
5,5-diCO2Et-oxathia
2-nPr—Ph
1-2066
O═
4-F-2-nPr—Ph
1-2067
S═
4-F-2-nPr—Ph
1-2068
cPr
4-F-2-nPr—Ph
1-2069
cBu
4-F-2-nPr—Ph
1-2070
cPent
4-F-2-nPr—Ph
1-2071
cHex
4-F-2-nPr—Ph
1-2072
cHept
4-F-2-nPr—Ph
1-2073
oxi
4-F-2-nPr—Ph
1-2074
oxe
4-F-2-nPr—Ph
1-2075
oxo
4-F-2-nPr—Ph
1-2076
oxa
4-F-2-nPr—Ph
1-2077
dioxo
4-F-2-nPr—Ph
1-2078
dioxa
4-F-2-nPr—Ph
1-2079
dioxe
4-F-2-nPr—Ph
1-2080
dithio
4-F-2-nPr—Ph
1-2081
dithia
4-F-2-nPr—Ph
1-2082
ring 1
4-F-2-nPr—Ph
1-2083
ring 2
4-F-2-nPr—Ph
1-2084
oxathio
4-F-2-nPr—Ph
1-2085
oxathia
4-F-2-nPr—Ph
1-2086
ozl
4-F-2-nPr—Ph
1-2087
ozn
4-F-2-nPr—Ph
1-2088
tzl
4-F-2-nPr—Ph
1-2089
tzn
4-F-2-nPr—Ph
1-2090
3-HM-cPent
4-F-2-nPr—Ph
1-2091
4-HM-dioxo
4-F-2-nPr—Ph
1-2092
4-HM-dithio
4-F-2-nPr—Ph
1-2093
4-HM-oxathio
4-F-2-nPr—Ph
1-2094
3,4-diHM-cPent
4-F-2-nPr—Ph
1-2095
4,5-diHM-dioxo
4-F-2-nPr—Ph
1-2096
4,5-diHM-dithio
4-F-2-nPr—Ph
1-2097
4,5-diHM-oxathio
4-F-2-nPr—Ph
1-2098
3,4-diHE-cPent
4-F-2-nPr—Ph
1-2099
4,5-diHE-dioxo
4-F-2-nPr—Ph
1-2100
4,5-diHE-dithio
4-F-2-nPr—Ph
1-2101
4,5-diHE-oxathio
4-F-2-nPr—Ph
1-2102
3-HE-cPent
4-F-2-nPr—Ph
1-2103
4-HE-dioxo
4-F-2-nPr—Ph
1-2104
4-HE-dithio
4-F-2-nPr—Ph
1-2105
4-HE-oxathio
4-F-2-nPr—Ph
1-2106
3-HP-cPent
4-F-2-nPr—Ph
1-2107
4-HP-dioxo
4-F-2-nPr—Ph
1-2108
4-HP-dithio
4-F-2-nPr—Ph
1-2109
4-HP-oxathio
4-F-2-nPr—Ph
1-2110
3-HB-cPent
4-F-2-nPr—Ph
1-2111
4-HB-dioxo
4-F-2-nPr—Ph
1-2112
4-HB-dithio
4-F-2-nPr—Ph
1-2113
4-HB-oxathio
4-F-2-nPr—Ph
1-2114
ring 3
4-F-2-nPr—Ph
1-2115
ring 4
4-F-2-nPr—Ph
1-2116
ring 5
4-F-2-nPr—Ph
1-2117
ring 6
4-F-2-nPr—Ph
1-2118
ring 7
4-F-2-nPr—Ph
1-2119
ring 8
4-F-2-nPr—Ph
1-2120
ring 9
4-F-2-nPr—Ph
1-2121
ring 10
4-F-2-nPr—Ph
1-2122
3,4-diCH2NHAc-cPent
4-F-2-nPr—Ph
1-2123
4,5-diCH2NHAc-dioxo
4-F-2-nPr—Ph
1-2124
4,5-diCH2NHAc-dithio
4-F-2-nPr—Ph
1-2125
4,5-diCH2NHAc-oxathio
4-F-2-nPr—Ph
1-2126
ring 11
4-F-2-nPr—Ph
1-2127
ring 12
4-F-2-nPr—Ph
1-2128
ring 13
4-F-2-nPr—Ph
1-2129
ring 14
4-F-2-nPr—Ph
1-2130
4-OH-cHex
4-F-2-nPr—Ph
1-2131
5-OH-dioxa
4-F-2-nPr—Ph
1-2132
5-OH-dithia
4-F-2-nPr—Ph
1-2133
5-OH-oxathia
4-F-2-nPr—Ph
1-2134
4-NHAc-cHex
4-F-2-nPr—Ph
1-2135
5-NHAc-dioxa
4-F-2-nPr—Ph
1-2136
5-NHAc-dithia
4-F-2-nPr—Ph
1-2137
5-NHAc-oxathia
4-F-2-nPr—Ph
1-2138
4,4-diMe-cHex
4-F-2-nPr—Ph
1-2139
5,5-diMe-dioxa
4-F-2-nPr—Ph
1-2140
5,5-diMe-dithia
4-F-2-nPr—Ph
1-2141
5,5-diMe-oxathia
4-F-2-nPr—Ph
1-2142
4,4-diHM-cHex
4-F-2-nPr—Ph
1-2143
5,5-diHM-dioxa
4-F-2-nPr—Ph
1-2144
5,5-diHM-dithia
4-F-2-nPr—Ph
1-2145
5,5-diHM-oxathia
4-F-2-nPr—Ph
1-2146
ring 15
4-F-2-nPr—Ph
1-2147
ring 16
4-F-2-nPr—Ph
1-2148
ring 17
4-F-2-nPr—Ph
1-2149
ring 18
4-F-2-nPr—Ph
1-2150
4,4-diCO2Et-cHex
4-F-2-nPr—Ph
1-2151
5,5-diCO2Et-dioxa
4-F-2-nPr—Ph
1-2152
5,5-diCO2Et-dithia
4-F-2-nPr—Ph
1-2153
5,5-diCO2Et-oxathia
4-F-2-nPr—Ph
1-2154
ring 19
2-Cl—Ph
1-2155
ring 20
2-Cl—Ph
1-2156
ring 21
2-Cl—Ph
1-2157
ring 19
2-Br—Ph
1-2158
ring 20
2-Br—Ph
1-2159
ring 21
2-Br—Ph
1-2160
ring 19
2-Cl-6-Me—Ph
1-2161
ring 20
2-Cl-6-Me—Ph
1-2162
ring 21
2-Cl-6-Me—Ph
1-2163
ring 19
2-Cl-4-F—Ph
1-2164
ring 20
2-Cl-4-F—Ph
1-2165
ring 21
2-Cl-4-F—Ph
1-2166
ring 19
2,4-diF
1-2167
ring 20
2,4-diF
1-2168
ring 21
2,4-diF
1-2169
ring 19
2-Br-4-F—Ph
1-2170
ring 20
2-Br-4-F—Ph
1-2171
ring 21
2-Br-4-F—Ph
1-2172
ring 19
2-nBu-4-F—Ph
1-2173
ring 20
2-nBu-4-F—Ph
1-2174
ring 21
2-nBu-4-F—Ph
1-2175
ring 19
2-nPent-Ph
1-2176
ring 20
2-nPent-Ph
1-2177
ring 21
2-nPent-Ph
1-2178
ring 19
4-F-2-nPent-Ph
1-2179
ring 20
4-F-2-nPent-Ph
1-2180
ring 21
4-F-2-nPent-Ph
1-2181
ring 19
2-nHex—Ph
1-2182
ring 20
2-nHex—Ph
1-2183
ring 21
2-nHex—Ph
1-2184
ring 19
4-F-2-nHex—Ph
1-2185
ring 20
4-F-2-nHex—Ph
1-2186
ring 21
4-F-2-nHex—Ph
1-2187
ring 19
2-nHept-Ph
1-2188
ring 20
2-nHept-Ph
1-2189
ring 21
2-nHept-Ph
1-2190
ring 19
4-F-2-nHept-Ph
1-2191
ring 20
4-F-2-nHept-Ph
1-2192
ring 21
4-F-2-nHept-Ph
1-2193
ring 19
2-nOct-Ph
1-2194
ring 20
2-nOct-Ph
1-2195
ring 21
2-nOct-Ph
1-2196
ring 19
4-F-2-nOct-Ph
1-2197
ring 20
4-F-2-nOct-Ph
1-2198
ring 21
4-F-2-nOct-Ph
1-2199
ring 19
Ph
1-2200
ring 20
Ph
1-2201
ring 21
Ph
1-2202
ring 19
4-F—Ph
1-2203
ring 20
4-F—Ph
1-2204
ring 21
4-F—Ph
1-2205
ring 19
2-Cl-4-Me—Ph
1-2206
ring 20
2-Cl-4-Me—Ph
1-2207
ring 21
2-Cl-4-Me—Ph
1-2208
ring 19
2-nBu—Ph
1-2209
ring 20
2-nBu—Ph
1-2210
ring 21
2-nBu—Ph
1-2211
ring 19
2-nPr—Ph
1-2212
ring 20
2-nPr—Ph
1-2213
ring 21
2-nPr—Ph
1-2214
ring 19
4-F-2-nPr—Ph
1-2215
ring 20
4-F-2-nPr—Ph
1-2216
ring 21
4-F-2-nPr—Ph
1-2217
dioxo
2-F—Ph
1-2218
4-HM-dioxo
2-F—Ph
1-2219
4,5-diHM-dioxo
2-F—Ph
1-2220
4,5-diHE-dioxo
2-F—Ph
1-2221
ring 19
2-F—Ph
1-2222
ring 20
2-F—Ph
1-2223
ring 21
2-F—Ph
1-2224
dioxo
2-I—Ph
1-2225
4-HM-dioxo
2-I—Ph
1-2226
4,5-diHM-dioxo
2-I—Ph
1-2227
4,5-diHE-dioxo
2-I—Ph
1-2228
ring 19
2-I—Ph
1-2229
ring 20
2-I—Ph
1-2230
ring 21
2-I—Ph
1-2231
dioxo
4-Cl—Ph
1-2232
4-HM-dioxo
4-Cl—Ph
1-2233
4,5-diHM-dioxo
4-Cl—Ph
1-2234
4,5-diHE-dioxo
4-Cl—Ph
1-2235
ring 19
4-Cl—Ph
1-2236
ring 20
4-Cl—Ph
1-2237
ring 21
4-Cl—Ph
1-2238
dioxo
2-Me—Ph
1-2239
4-HM-dioxo
2-Me—Ph
1-2240
4,5-diHM-dioxo
2-Me—Ph
1-2241
4,5-diHE-dioxo
2-Me—Ph
1-2242
ring 19
2-Me—Ph
1-2243
ring 20
2-Me—Ph
1-2244
ring 21
2-Me—Ph
1-2245
dioxo
2-Et—Ph
1-2246
4-HM-dioxo
2-Et—Ph
1-2247
4,5-diHM-dioxo
2-Et—Ph
1-2248
4,5-diHE-dioxo
2-Et—Ph
1-2249
ring 19
2-Et—Ph
1-2250
ring 20
2-Et—Ph
1-2251
ring 21
2-Et—Ph
1-2252
dioxo
2-C≡CH—Ph
1-2253
4-HM-dioxo
2-C≡CH—Ph
1-2254
4,5-diHM-dioxo
2-C≡CH—Ph
1-2255
4,5-diHE-dioxo
2-C≡CH—Ph
1-2256
ring 19
2-C≡CH—Ph
1-2257
ring 20
2-C≡CH—Ph
1-2258
ring 21
2-C≡CH—Ph
1-2259
dioxo
2-iPr—Ph
1-2260
4-HM-dioxo
2-iPr—Ph
1-2261
4,5-diHM-dioxo
2-iPr—Ph
1-2262
4,5-diHE-dioxo
2-iPr—Ph
1-2263
ring 19
2-iPr—Ph
1-2264
ring 20
2-iPr—Ph
1-2265
ring 21
2-iPr—Ph
1-2266
dioxo
2-tBu—Ph
1-2267
4-HM-dioxo
2-tBu—Ph
1-2268
4,5-diHM-dioxo
2-tBu—Ph
1-2269
4,5-diHE-dioxo
2-tBu—Ph
1-2270
ring 19
2-tBu—Ph
1-2271
ring 20
2-tBu—Ph
1-2272
ring 21
2-tBu—Ph
1-2273
dioxo
2-sBu—Ph
1-2274
4-HM-dioxo
2-sBu—Ph
1-2275
4,5-diHM-dioxo
2-sBu—Ph
1-2276
4,5-diHE-dioxo
2-sBu—Ph
1-2277
ring 19
2-sBu—Ph
1-2278
ring 20
2-sBu—Ph
1-2279
ring 21
2-sBu—Ph
1-2280
dioxo
2-OMe—Ph
1-2281
4-HM-dioxo
2-OMe—Ph
1-2282
4,5-diHM-dioxo
2-OMe—Ph
1-2283
4,5-diHE-dioxo
2-OMe—Ph
1-2284
ring 19
2-OMe—Ph
1-2285
ring 20
2-OMe—Ph
1-2286
ring 21
2-OMe—Ph
1-2287
dioxo
2-OEt—Ph
1-2288
4-HM-dioxo
2-OEt—Ph
1-2289
4,5-diHM-dioxo
2-OEt—Ph
1-2290
4,5-diHE-dioxo
2-OEt—Ph
1-2291
ring 19
2-OEt—Ph
1-2292
ring 20
2-OEt—Ph
1-2293
ring 21
2-OEt—Ph
1-2294
dioxo
2-OCHF2—Ph
1-2295
4-HM-dioxo
2-OCHF2—Ph
1-2296
4,5-diHM-dioxo
2-OCHF2—Ph
1-2297
4,5-diHE-dioxo
2-OCHF2—Ph
1-2298
ring 19
2-OCHF2—Ph
1-2299
ring 20
2-OCHF2—Ph
1-2300
ring 21
2-OCHF2—Ph
1-2301
dioxo
2-SMe—Ph
1-2302
4-HM-dioxo
2-SMe—Ph
1-2303
4,5-diHM-dioxo
2-SMe—Ph
1-2304
4,5-diHE-dioxo
2-SMe—Ph
1-2305
ring 19
2-SMe—Ph
1-2306
ring 20
2-SMe—Ph
1-2307
ring 21
2-SMe—Ph
1-2308
dioxo
2-Ac—Ph
1-2309
4-HM-dioxo
2-Ac—Ph
1-2310
4,5-diHM-dioxo
2-Ac—Ph
1-2311
4,5-diHE-dioxo
2-Ac—Ph
1-2312
ring 19
2-Ac—Ph
1-2313
ring 20
2-Ac—Ph
1-2314
ring 21
2-Ac—Ph
1-2315
dioxo
2-Bn—Ph
1-2316
4-HM-dioxo
2-Bn—Ph
1-2317
4,5-diHM-dioxo
2-Bn—Ph
1-2318
4,5-diHE-dioxo
2-Bn—Ph
1-2319
ring 19
2-Bn—Ph
1-2320
ring 20
2-Bn—Ph
1-2321
ring 21
2-Bn—Ph
1-2322
dioxo
2-Mor-Ph
1-2323
4-HM-dioxo
2-Mor-Ph
1-2324
4,5-diHM-dioxo
2-Mor-Ph
1-2325
4,5-diHE-dioxo
2-Mor-Ph
1-2326
ring 19
2-Mor-Ph
1-2327
ring 20
2-Mor-Ph
1-2328
ring 21
2-Mor-Ph
1-2329
dioxo
Flu
1-2330
4-HM-dioxo
Flu
1-2331
4,5-diHM-dioxo
Flu
1-2332
4,5-diHE-dioxo
Flu
1-2333
ring 19
Flu
1-2334
ring 20
Flu
1-2335
ring 21
Flu
1-2336
dioxo
2-CH2CH2Pyrd-Ph
1-2337
4-HM-dioxo
2-CH2CH2Pyrd-Ph
1-2338
4,5-diHM-dioxo
2-CH2CH2Pyrd-Ph
1-2339
4,5-diHE-dioxo
2-CH2CH2Pyrd-Ph
1-2340
ring 19
2-CH2CH2Pyrd-Ph
1-2341
ring 20
2-CH2CH2Pyrd-Ph
1-2342
ring 21
2-CH2CH2Pyrd-Ph
1-2343
dioxo
2-CH2CH2NHBoc—Ph
1-2344
4-HM-dioxo
2-CH2CH2NHBoc—Ph
1-2345
4,5-diHM-dioxo
2-CH2CH2NHBoc—Ph
1-2346
4,5-diHE-dioxo
2-CH2CH2NHBoc—Ph
1-2347
ring 19
2-CH2CH2NHBoc—Ph
1-2348
ring 20
2-CH2CH2NHBoc—Ph
1-2349
ring 21
2-CH2CH2NHBoc—Ph
1-2350
dioxo
2-NH2—Ph
1-2351
4-HM-dioxo
2-NH2—Ph
1-2352
4,5-diHM-dioxo
2-NH2—Ph
1-2353
4,5-diHE-dioxo
2-NH2—Ph
1-2354
ring 19
2-NH2—Ph
1-2355
ring 20
2-NH2—Ph
1-2356
ring 21
2-NH2—Ph
1-2357
dioxo
4-F-2-Me—Ph
1-2358
4-HM-dioxo
4-F-2-Me—Ph
1-2359
4,5-diHM-dioxo
4-F-2-Me—Ph
1-2360
4,5-diHE-dioxo
4-F-2-Me—Ph
1-2361
ring 19
4-F-2-Me—Ph
1-2362
ring 20
4-F-2-Me—Ph
1-2363
ring 21
4-F-2-Me—Ph
1-2364
dioxo
3-Cl-4-F—Ph
1-2365
4-HM-dioxo
3-Cl-4-F—Ph
1-2366
4,5-diHM-dioxo
3-Cl-4-F—Ph
1-2367
4,5-diHE-dioxo
3-Cl-4-F—Ph
1-2368
ring 19
3-Cl-4-F—Ph
1-2369
ring 20
3-Cl-4-F—Ph
1-2370
ring 21
3-Cl-4-F—Ph
1-2371
dioxo
4-F-3-CF3—Ph
1-2372
4-HM-dioxo
4-F-3-CF3—Ph
1-2373
4,5-diHM-dioxo
4-F-3-CF3—Ph
1-2374
4,5-diHE-dioxo
4-F-3-CF3—Ph
1-2375
ring 19
4-F-3-CF3—Ph
1-2376
ring 20
4-F-3-CF3—Ph
1-2377
ring 21
4-F-3-CF3—Ph
1-2378
dioxo
4-F-3-OMe—Ph
1-2379
4-HM-dioxo
4-F-3-OMe—Ph
1-2380
4,5-diHM-dioxo
4-F-3-OMe—Ph
1-2381
4,5-diHE-dioxo
4-F-3-OMe—Ph
1-2382
ring 19
4-F-3-OMe—Ph
1-2383
ring 20
4-F-3-OMe—Ph
1-2384
ring 21
4-F-3-OMe—Ph
1-2385
dioxo
3,4-diF—Ph
1-2386
4-HM-dioxo
3,4-diF—Ph
1-2387
4,5-diHM-dioxo
3,4-diF—Ph
1-2388
4,5-diHE-dioxo
3,4-diF—Ph
1-2389
ring 19
3,4-diF—Ph
1-2390
ring 20
3,4-diF—Ph
1-2391
ring 21
3,4-diF—Ph
1-2392
dioxo
2,4-diOMe—Ph
1-2393
4-HM-dioxo
2,4-diOMe—Ph
1-2394
4,5-diHM-dioxo
2,4-diOMe—Ph
1-2395
4,5-diHE-dioxo
2,4-diOMe—Ph
1-2396
ring 19
2,4-diOMe—Ph
1-2397
ring 20
2,4-diOMe—Ph
1-2398
ring 21
2,4-diOMe—Ph
1-2399
dioxo
4-Cl-2-F—Ph
1-2400
4-HM-dioxo
4-Cl-2-F—Ph
1-2401
4,5-diHM-dioxo
4-Cl-2-F—Ph
1-2402
4,5-diHE-dioxo
4-Cl-2-F—Ph
1-2403
ring 19
4-Cl-2-F—Ph
1-2404
ring 20
4-Cl-2-F—Ph
1-2405
ring 21
4-Cl-2-F—Ph
1-2406
dioxo
2-Br-4-Cl—Ph
1-2407
4-HM-dioxo
2-Br-4-Cl—Ph
1-2408
4,5-diHM-dioxo
2-Br-4-Cl—Ph
1-2409
4,5-diHE-dioxo
2-Br-4-Cl—Ph
1-2410
ring 19
2-Br-4-Cl—Ph
1-2411
ring 20
2-Br-4-Cl—Ph
1-2412
ring 21
2-Br-4-Cl—Ph
1-2413
dioxo
4-Cl-2-Me—Ph
1-2414
4-HM-dioxo
4-Cl-2-Me—Ph
1-2415
4,5-diHM-dioxo
4-Cl-2-Me—Ph
1-2416
4,5-diHE-dioxo
4-Cl-2-Me—Ph
1-2417
ring 19
4-Cl-2-Me—Ph
1-2418
ring 20
4-Cl-2-Me—Ph
1-2419
ring 21
4-Cl-2-Me—Ph
1-2420
dioxo
4-Cl-2-CO2Me—Ph
1-2421
4-HM-dioxo
4-Cl-2-CO2Me—Ph
1-2422
4,5-diHM-dioxo
4-Cl-2-CO2Me—Ph
1-2423
4,5-diHE-dioxo
4-Cl-2-CO2Me—Ph
1-2424
ring 19
4-Cl-2-CO2Me—Ph
1-2425
ring 20
4-Cl-2-CO2Me—Ph
1-2426
ring 21
4-Cl-2-CO2Me—Ph
1-2427
dioxo
3,4-diCl—Ph
1-2428
4-HM-dioxo
3,4-diCl—Ph
1-2429
4,5-diHM-dioxo
3,4-diCl—Ph
1-2430
4,5-diHE-dioxo
3,4-diCl—Ph
1-2431
ring 19
3,4-diCl—Ph
1-2432
ring 20
3,4-diCl—Ph
1-2433
ring 21
3,4-diCl—Ph
1-2434
dioxo
2,5-diF—Ph
1-2435
4-HM-dioxo
2,5-diF—Ph
1-2436
4,5-diHM-dioxo
2,5-diF—Ph
1-2437
4,5-diHE-dioxo
2,5-diF—Ph
1-2438
ring 19
2,5-diF—Ph
1-2439
ring 20
2,5-diF—Ph
1-2440
ring 21
2,5-diF—Ph
1-2441
dioxo
2,6-diF—Ph
1-2442
4-HM-dioxo
2,6-diF—Ph
1-2443
4,5-diHM-dioxo
2,6-diF—Ph
1-2444
4,5-diHE-dioxo
2,6-diF—Ph
1-2445
ring 19
2,6-diF—Ph
1-2446
ring 20
2,6-diF—Ph
1-2447
ring 21
2,6-diF—Ph
1-2448
dioxo
2-F-4-Me—Ph
1-2449
4-HM-dioxo
2-F-4-Me—Ph
1-2450
4,5-diHM-dioxo
2-F-4-Me—Ph
1-2451
4,5-diHE-dioxo
2-F-4-Me—Ph
1-2452
ring 19
2-F-4-Me—Ph
1-2453
ring 20
2-F-4-Me—Ph
1-2454
ring 21
2-F-4-Me—Ph
1-2455
dioxo
2-F-5-Me—Ph
1-2456
4-HM-dioxo
2-F-5-Me—Ph
1-2457
4,5-diHM-dioxo
2-F-5-Me—Ph
1-2458
4,5-diHE-dioxo
2-F-5-Me—Ph
1-2459
ring 19
2-F-5-Me—Ph
1-2460
ring 20
2-F-5-Me—Ph
1-2461
ring 21
2-F-5-Me—Ph
1-2462
dioxo
2-F-4-OMe—Ph
1-2463
4-HM-dioxo
2-F-4-OMe—Ph
1-2464
4,5-diHM-dioxo
2-F-4-OMe—Ph
1-2465
4,5-diHE-dioxo
2-F-4-OMe—Ph
1-2466
ring 19
2-F-4-OMe—Ph
1-2467
ring 20
2-F-4-OMe—Ph
1-2468
ring 21
2-F-4-OMe—Ph
1-2469
dioxo
5-Cl-2-F—Ph
1-2470
4-HM-dioxo
5-Cl-2-F—Ph
1-2471
4,5-diHM-dioxo
5-Cl-2-F—Ph
1-2472
4,5-diHE-dioxo
5-Cl-2-F—Ph
1-2473
ring 19
5-Cl-2-F—Ph
1-2474
ring 20
5-Cl-2-F—Ph
1-2475
ring 21
5-Cl-2-F—Ph
1-2476
dioxo
2,3,4-triF—Ph
1-2477
4-HM-dioxo
2,3,4-triF—Ph
1-2478
4,5-diHM-dioxo
2,3,4-triF—Ph
1-2479
4,5-diHE-dioxo
2,3,4-triF—Ph
1-2480
ring 19
2,3,4-triF—Ph
1-2481
ring 20
2,3,4-triF—Ph
1-2482
ring 21
2,3,4-triF—Ph
1-2483
dioxo
2,4,5-triF—Ph
1-2484
4-HM-dioxo
2,4,5-triF—Ph
1-2485
4,5-diHM-dioxo
2,4,5-triF—Ph
1-2486
4,5-diHE-dioxo
2,4,5-triF—Ph
1-2487
ring 19
2,4,5-triF—Ph
1-2488
ring 20
2,4,5-triF—Ph
1-2489
ring 21
2,4,5-triF—Ph
1-2490
dioxo
2,4,6-triF—Ph
1-2491
4-HM-dioxo
2,4,6-triF—Ph
1-2492
4,5-diHM-dioxo
2,4,6-triF—Ph
1-2493
4,5-diHE-dioxo
2,4,6-triF—Ph
1-2494
ring 19
2,4,6-triF—Ph
1-2495
ring 20
2,4,6-triF—Ph
1-2496
ring 21
2,4,6-triF—Ph
1-2497
dioxo
2,4-diCl—Ph
1-2498
4-HM-dioxo
2,4-diCl—Ph
1-2499
4,5-diHM-dioxo
2,4-diCl—Ph
1-2500
4,5-diHE-dioxo
2,4-diCl—Ph
1-2501
ring 19
2,4-diCl—Ph
1-2502
ring 20
2,4-diCl—Ph
1-2503
ring 21
2,4-diCl—Ph
1-2504
dioxo
4-Br-2-Cl—Ph
1-2505
4-HM-dioxo
4-Br-2-Cl—Ph
1-2506
4,5-diHM-dioxo
4-Br-2-Cl—Ph
1-2507
4,5-diHE-dioxo
4-Br-2-Cl—Ph
1-2508
ring 19
4-Br-2-Cl—Ph
1-2509
ring 20
4-Br-2-Cl—Ph
1-2510
ring 21
4-Br-2-Cl—Ph
1-2511
dioxo
4-tBu-2-Cl—Ph
1-2512
4-HM-dioxo
4-tBu-2-Cl—Ph
1-2513
4,5-diHM-dioxo
4-tBu-2-Cl—Ph
1-2514
4,5-diHE-dioxo
4-tBu-2-Cl—Ph
1-2515
ring 19
4-tBu-2-Cl—Ph
1-2516
ring 20
4-tBu-2-Cl—Ph
1-2517
ring 21
4-tBu-2-Cl—Ph
1-2518
dioxo
2-Cl-6-F—Ph
1-2519
4-HM-dioxo
2-Cl-6-F—Ph
1-2520
4,5-diHM-dioxo
2-Cl-6-F—Ph
1-2521
4,5-diHE-dioxo
2-Cl-6-F—Ph
1-2522
ring 19
2-Cl-6-F—Ph
1-2523
ring 20
2-Cl-6-F—Ph
1-2524
ring 21
2-Cl-6-F—Ph
1-2525
dioxo
2,6-diCl—Ph
1-2526
4-HM-dioxo
2,6-diCl—Ph
1-2527
4,5-diHM-dioxo
2,6-diCl—Ph
1-2528
4,5-diHE-dioxo
2,6-diCl—Ph
1-2529
ring 19
2,6-diCl—Ph
1-2530
ring 20
2,6-diCl—Ph
1-2531
ring 21
2,6-diCl—Ph
1-2532
dioxo
2,3-diCl—Ph
1-2533
4-HM-dioxo
2,3-diCl—Ph
1-2534
4,5-diHM-dioxo
2,3-diCl—Ph
1-2535
4,5-diHE-dioxo
2,3-diCl—Ph
1-2536
ring 19
2,3-diCl—Ph
1-2537
ring 20
2,3-diCl—Ph
1-2538
ring 21
2,3-diCl—Ph
1-2539
dioxo
2,5-diCl—Ph
1-2540
4-HM-dioxo
2,5-diCl—Ph
1-2541
4,5-diHM-dioxo
2,5-diCl—Ph
1-2542
4,5-diHE-dioxo
2,5-diCl—Ph
1-2543
ring 19
2,5-diCl—Ph
1-2544
ring 20
2,5-diCl—Ph
1-2545
ring 21
2,5-diCl—Ph
1-2546
dioxo
2-Cl-4,6-diF—Ph
1-2547
4-HM-dioxo
2-Cl-4,6-diF—Ph
1-2548
4,5-diHM-dioxo
2-Cl-4,6-diF—Ph
1-2549
4,5-diHE-dioxo
2-Cl-4,6-diF—Ph
1-2550
ring 19
2-Cl-4,6-diF—Ph
1-2551
ring 20
2-Cl-4,6-diF—Ph
1-2552
ring 21
2-Cl-4,6-diF—Ph
1-2553
dioxo
2,6-diCl-4-F—Ph
1-2554
4-HM-dioxo
2,6-diCl-4-F—Ph
1-2555
4,5-diHM-dioxo
2,6-diCl-4-F—Ph
1-2556
4,5-diHE-dioxo
2,6-diCl-4-F—Ph
1-2557
ring 19
2,6-diCl-4-F—Ph
1-2558
ring 20
2,6-diCl-4-F—Ph
1-2559
ring 21
2,6-diCl-4-F—Ph
1-2560
dioxo
2-Br-6-Cl-4-F—Ph
1-2561
4-HM-dioxo
2-Br-6-Cl-4-F—Ph
1-2562
4,5-diHM-dioxo
2-Br-6-Cl-4-F—Ph
1-2563
4,5-diHE-dioxo
2-Br-6-Cl-4-F—Ph
1-2564
ring 19
2-Br-6-Cl-4-F—Ph
1-2565
ring 20
2-Br-6-Cl-4-F—Ph
1-2566
ring 21
2-Br-6-Cl-4-F—Ph
1-2567
dioxo
4-Cl-2-OMe-5-Me—Ph
1-2568
4-HM-dioxo
4-Cl-2-OMe-5-Me—Ph
1-2569
4,5-diHM-dioxo
4-Cl-2-OMe-5-Me—Ph
1-2570
4,5-diHE-dioxo
4-Cl-2-OMe-5-Me—Ph
1-2571
ring 19
4-Cl-2-OMe-5-Me—Ph
1-2572
ring 20
4-Cl-2-OMe-5-Me—Ph
1-2573
ring 21
4-Cl-2-OMe-5-Me—Ph
1-2574
dioxo
2,4-diBr—Ph
1-2575
4-HM-dioxo
2,4-diBr—Ph
1-2576
4,5-diHM-dioxo
2,4-diBr—Ph
1-2577
4,5-diHE-dioxo
2,4-diBr—Ph
1-2578
ring 19
2,4-diBr—Ph
1-2579
ring 20
2,4-diBr—Ph
1-2580
ring 21
2,4-diBr—Ph
1-2581
dioxo
2,6-diBr—Ph
1-2582
4-HM-dioxo
2,6-diBr—Ph
1-2583
4,5-diHM-dioxo
2,6-diBr—Ph
1-2584
4,5-diHE-dioxo
2,6-diBr—Ph
1-2585
ring 19
2,6-diBr—Ph
1-2586
ring 20
2,6-diBr—Ph
1-2587
ring 21
2,6-diBr—Ph
1-2588
dioxo
2-Br-4-iPr—Ph
1-2589
4-HM-dioxo
2-Br-4-iPr—Ph
1-2590
4,5-diHM-dioxo
2-Br-4-iPr—Ph
1-2591
4,5-diHE-dioxo
2-Br-4-iPr—Ph
1-2592
ring 19
2-Br-4-iPr—Ph
1-2593
ring 20
2-Br-4-iPr—Ph
1-2594
ring 21
2-Br-4-iPr—Ph
1-2595
dioxo
2-nNon-Ph
1-2596
4-HM-dioxo
2-nNon-Ph
1-2597
4,5-diHM-dioxo
2-nNon-Ph
1-2598
4,5-diHE-dioxo
2-nNon-Ph
1-2599
ring 19
2-nNon-Ph
1-2600
ring 20
2-nNon-Ph
1-2601
ring 21
2-nNon-Ph
1-2602
dioxo
4-F-2-nNon-Ph
1-2603
4-HM-dioxo
4-F-2-nNon-Ph
1-2604
4,5-diHM-dioxo
4-F-2-nNon-Ph
1-2605
4,5-diHE-dioxo
4-F-2-nNon-Ph
1-2606
ring 19
4-F-2-nNon-Ph
1-2607
ring 20
4-F-2-nNon-Ph
1-2608
ring 21
4-F-2-nNon-Ph
1-2609
dioxo
2-nDec-Ph
1-2610
4-HM-dioxo
2-nDec-Ph
1-2611
4,5-diHM-dioxo
2-nDec-Ph
1-2612
4,5-diHE-dioxo
2-nDec-Ph
1-2613
ring 19
2-nDec-Ph
1-2614
ring 20
2-nDec-Ph
1-2615
ring 21
2-nDec-Ph
1-2616
dioxo
4-F-2-nDec-Ph
1-2617
4-HM-dioxo
4-F-2-nDec-Ph
1-2618
4,5-diHM-dioxo
4-F-2-nDec-Ph
1-2619
4,5-diHE-dioxo
4-F-2-nDec-Ph
1-2620
ring 19
4-F-2-nDec-Ph
1-2621
ring 20
4-F-2-nDec-Ph
1-2622
ring 21
4-F-2-nDec-Ph
1-2623
dioxo
2-Et-4-F—Ph
1-2624
4-HM-dioxo
2-Et-4-F—Ph
1-2625
4,5-diHM-dioxo
2-Et-4-F—Ph
1-2626
4,5-diHE-dioxo
2-Et-4-F—Ph
1-2627
ring 19
2-Et-4-F—Ph
1-2628
ring 20
2-Et-4-F—Ph
1-2629
ring 21
2-Et-4-F—Ph
TABLE 2
##STR00010##
Compound
No.
X, Y
R3
2-1
dioxo
2-Cl—Ph
2-2
4-HM-dioxo
2-Cl—Ph
2-3
4,5 -diHM-dioxo
2-Cl—Ph
2-4
4,5 -diHE-dioxo
2-Cl—Ph
2-5
dioxo
2-Br—Ph
2-6
4-HM-dioxo
2-Br—Ph
2-7
4,5 -diHM-dioxo
2-Br—Ph
2-8
4,5-diHE-dioxo
2-Br—Ph
2-9
dioxo
2-Cl-6-Me—Ph
2-10
4-HM-dioxo
2-Cl-6-Me—Ph
2-11
4,5-diHM-dioxo
2-Cl-6-Me—Ph
2-12
4,5-diHE-dioxo
2-Cl-6-Me—Ph
2-13
dioxo
2-Cl-4-F—Ph
2-14
4-HM-dioxo
2-Cl-4-F—Ph
2-15
4,5-diHM-dioxo
2-Cl-4-F—Ph
2-16
4,5-diHE-dioxo
2-Cl-4-F—Ph
2-17
dioxo
2,4-diF
2-18
4-HM-dioxo
2,4-diF
2-19
4,5-diHM-dioxo
2,4-diF
2-20
4,5-diHE-dioxo
2,4-diF
2-21
dioxo
2-Br-4-F Ph
2-22
4-HM-dioxo
2-Br-4-F Ph
2-23
4,5-diHM-dioxo
2-Br-4-F Ph
2-24
4,5-diHE-dioxo
2-Br-4-F Ph
2-25
dioxo
2-nBu-4-F Ph
2-26
4-HM-dioxo
2-nBu-4-F Ph
2-27
4,5-diHM-dioxo
2-nBu-4-F Ph
2-28
4,5-diHE-dioxo
2-nBu-4-F Ph
2-29
dioxo
2-nPent-Ph
2-30
4-HM-dioxo
2-nPent-Ph
2-31
4,5-diHM-dioxo
2-nPent-Ph
2-32
4,5-diHE-dioxo
2-nPent-Ph
2-33
dioxo
4-F-2-nPent-Ph
2-34
4-HM-dioxo
4-F-2-nPent-Ph
2-35
4,5-diHM-dioxo
4-F-2-nPent-Ph
2-35
4,5-diHE-dioxo
4-F-2-nPent-Ph
2-37
dioxo
2-nHex—Ph
2-38
4-HM-dioxo
2-nHex—Ph
2-39
4,5-diHM-dioxo
2-nHex—Ph
2-40
4,5-diHE-dioxo
2-nHex—Ph
2-41
dioxo
4-F-2-nHex Ph
2-42
4-HM-dioxo
4-F-2-nHex Ph
2-43
4,5-diHM-dioxo
4-F-2-nHex Ph
2-44
4,5-diHE-dioxo
4-F-2-nHex Ph
2-45
dioxo
2-nHept-Ph
2-46
4-HM-dioxo
2-nHept-Ph
2-47
4,5-diHM-dioxo
2-nHept-Ph
2-48
4,5-diHE-dioxo
2-nHept-Ph
2-49
dioxo
4-F-2-nHept-Ph
2-50
4-HM-dioxo
4-F-2-nHept-Ph
2-51
4,5-diHM-dioxo
4-F-2-nHept-Ph
2-52
4,5-diHE-dioxo
4-F-2-nHept-Ph
2-53
dioxo
2-nOct-Ph
2-54
4-HM-dioxo
2-nOct-Ph
2-55
4,5-diHM-dioxo
2-nOct-Ph
2-56
4,5-diHE-dioxo
2-nOct-Ph
2-57
dioxo
4-F-2-nOct-Ph
2-58
4-HM-dioxo
4-F-2-nOct-Ph
2-59
4,5-diHM-dioxo
4-F-2-nOct-Ph
2-60
4,5-diHE-dioxo
4-F-2-nOct-Ph
2-61
dioxo
Ph
2-62
4-HM-dioxo
Ph
2-63
4,5-diHM-dioxo
Ph
2-64
4,5-diHE-dioxo
Ph
2-65
dioxo
4-F—Ph
2-66
4-HM-dioxo
4-F—Ph
2-67
4,5-diHM-dioxo
4-F—Ph
2-68
4,5-diHE-dioxo
4-F—Ph
2-69
dioxo
2-Cl-4-Me Ph
2-70
4-HM-dioxo
2-Cl-4-Me Ph
2-71
4,5-diHM-dioxo
2-Cl-4-Me Ph
2-72
4,5-diHE-dioxo
2-Cl-4-Me Ph
2-73
dioxo
2-nBu—Ph
2-74
4-HM-dioxo
2-nBu—Ph
2-75
4,5-diHM-dioxo
2-nBu—Ph
2-76
4,5-diHE-dioxo
2-nBu—Ph
2-77
dioxo
2-nPr—Ph
2-78
4-HM-dioxo
2-nPr—Ph
2-79
4,5-diHM-dioxo
2-nPr—Ph
2-80
4,5-diHE-dioxo
2-nPr—Ph
2-81
dioxo
4-F-2-nPr—Ph
2-82
4-HM-dioxo
4-F-2-nPr—Ph
2-83
4,5-diHM-dioxo
4-F-2-nPr—Ph
2-84
4,5-diHE-dioxo
4-F-2-nPr—Ph
TABLE 3
##STR00011##
Compound
No.
X, Y
R2
R3
3-1
dioxo
Me
2-Cl—Ph
3-2
4-HM-dioxo
Me
2-Cl—Ph
3-3
4,5-diHM-dioxo
Me
2-Cl—Ph
3-4
4,5-diHE-dioxo
Me
2-Cl—Ph
3-5
dioxo
nPr
2-Cl—Ph
3-6
4-HM-dioxo
nPr
2-Cl—Ph
3-7
4,5-diHM-dioxo
nPr
2-Cl—Ph
3-8
4,5-diHE-dioxo
nPr
2-Cl—Ph
3-9
dioxo
nBu
2-Cl—Ph
3-10
4-HM-dioxo
nBu
2-Cl—Ph
3-11
4,5-diHM-dioxo
nBu
2-Cl—Ph
3-12
4,5-diHE-dioxo
nBu
2-Cl—Ph
3-13
dioxo
iPr
2-Cl—Ph
3-14
4-HM-dioxo
iPr
2-Cl—Ph
3-15
4,5-diHM-dioxo
iPr
2-Cl—Ph
3-16
4,5-diHE-dioxo
iPr
2-Cl—Ph
3-17
dioxo
tBu
2-Cl—Ph
3-18
4-HM-dioxo
tBu
2-Cl—Ph
3-19
4,5-diHM-dioxo
tBu
2-Cl—Ph
3-20
4,5-diHE-dioxo
tBu
2-Cl—Ph
3-21
dioxo
CH2OAc
2-Cl—Ph
3-22
4-HM-dioxo
CH2OAc
2-Cl—Ph
3-23
4,5-diHM-dioxo
CH2OAc
2-Cl—Ph
3-24
4,5-diHE-dioxo
CH2OAc
2-Cl—Ph
3-25
dioxo
Me
2-Br—Ph
3-26
4-HM-dioxo
Me
2-Br—Ph
3-27
4,5-diHM-dioxo
Me
2-Br—Ph
3-28
4,5-diHE-dioxo
Me
2-Br—Ph
3-29
dioxo
nPr
2-Br—Ph
3-30
4-HM-dioxo
nPr
2-Br—Ph
3-31
4,5-diHM-dioxo
nPr
2-Br—Ph
3-32
4,5-diHE-dioxo
nPr
2-Br—Ph
3-33
dioxo
nBu
2-Br—Ph
3-34
4-HM-dioxo
nBu
2-Br—Ph
3-35
4,5-diHM-dioxo
nBu
2-Br—Ph
3-36
4,5-diHE-dioxo
nBu
2-Br—Ph
3-37
dioxo
iPr
2-Br—Ph
3-38
4-HM-dioxo
iPr
2-Br—Ph
3-39
4,5-diHM-dioxo
iPr
2-Br—Ph
3-40
4,5-diHE-d oxo
iPr
2-Br—Ph
3-41
dioxo
tBu
2-Br—Ph
3-42
4-HM-dioxo
tBu
2-Br—Ph
3-43
4,5-diHM-dioxo
tBu
2-Br—Ph
3-44
4,5-diHE-dioxo
tBu
2-Br—Ph
3-45
dioxo
CH2OAc
2-Br—Ph
3-45
4-HM-dioxo
CH2OAc
2-Br—Ph
3-47
4,5-diHM-dioxo
CH2OAc
2-Br—Ph
3-48
4,5-diHE-dioxo
CH2OAc
2-Br—Ph
3-49
dioxo
Me
2-Cl-6-Me—Ph
3-50
4-HM-dioxo
Me
2-Cl-6-Me—Ph
3-51
4,5-diHM-dioxo
Me
2-Cl-6-Me—Ph
3-52
4,5-diHE-dioxo
Me
2-Cl-6-Me—Ph
3-53
dioxo
nPr
2-Cl-6-Me—Ph
3-54
4-HM-dioxo
nPr
2-Cl-6-Me—Ph
3-55
4,5-diHM-dioxo
nPr
2-Cl-6-Me—Ph
3-56
4,5-diHE-dioxo
nPr
2-Cl-6-Me—Ph
3-57
dioxo
nBu
2-Cl-6-Me—Ph
3-58
4-HM-dioxo
nBu
2-Cl-6-Me—Ph
3-59
4,5-diHM-dioxo
nBu
2-Cl-6-Me—Ph
3-60
4,5-diHE-dioxo
nBu
2-Cl-6-Me—Ph
3-61
dioxo
iPr
2-Cl-6-Me—Ph
3-62
4-HM-dioxo
iPr
2-Cl-6-Me—Ph
3-63
4,5-diHM-dioxo
iPr
2-Cl-6-Me—Ph
3-64
4,5-diHE-dioxo
iPr
2-Cl-6-Me—Ph
3-65
dioxo
tBu
2-Cl-6-Me—Ph
3-66
4-HM-dioxo
tBu
2-Cl-6-Me—Ph
3-67
4,5-diHM-dioxo
tBu
2-Cl-6-Me—Ph
3-68
4,5-diHE-dioxo
tBu
2-Cl-6-Me—Ph
3-69
dioxo
CH2OAc
2-Cl-6-Me—Ph
3-70
4-HM-dioxo
CH2OAc
2-Cl-6-Me—Ph
3-71
4,5-diHM-dioxo
CH2OAc
2-Cl-6-Me—Ph
3-72
4,5-diHE-dioxo
CH2OAc
2-Cl-6-Me—Ph
3-73
dioxo
Me
2-Cl-4-F—Ph
3-74
4-HM-dioxo
Me
2-Cl-4-F—Ph
3-75
4,5-diHM-dioxo
Me
2-Cl-4-F—Ph
3-76
4,5-diHE-dioxo
Me
2-Cl-4-F—Ph
3-77
dioxo
nPr
2-Cl-4-F—Ph
3-78
4-HM-dioxo
nPr
2-Cl-4-F—Ph
3-79
4,5-diHM-dioxo
nPr
2-Cl-4-F—Ph
3-80
4,5-diHE-dioxo
nPr
2-Cl-4-F—Ph
3-81
dioxo
nBu
2-Cl-4-F—Ph
3-82
4-HM-dioxo
nBu
2-Cl-4-F—Ph
3-83
4,5-diHM-dioxo
nBu
2-Cl-4-F—Ph
3-84
4,5-diHE-dioxo
nBu
2-Cl-4-F—Ph
3-85
dioxo
iPr
2-Cl-4-F—Ph
3-86
4-HM-dioxo
iPr
2-Cl-4-F—Ph
3-87
4,5-diHM-dioxo
iPr
2-Cl-4-F—Ph
3-88
4,5-diHE-dioxo
iPr
2-Cl-4-F—Ph
3-89
dioxo
tBu
2-Cl-4-F—Ph
3-90
4-HM-dioxo
tBu
2-Cl-4-F—Ph
3-91
4,5-diHM-dioxo
tBu
2-Cl-4-F—Ph
3-92
4,5-diHE-dioxo
tBu
2-Cl-4-F—Ph
3-93
dioxo
CH2OAc
2-Cl-4-F—Ph
3-94
4-HM-dioxo
CH2OAc
2-Cl-4-F—Ph
3-95
4,5-diHM-dioxo
CH2OAc
2-Cl-4-F—Ph
3-96
4,5-diHE-dioxo
CH2OAc
2-Cl-4-F—Ph
3-97
dioxo
Me
2,4-diF—Ph
3-98
4-HM-dioxo
Me
2,4-diF—Ph
3-99
4,5-diHM-dioxo
Me
2,4-diF—Ph
3-100
4,5-diHE-dioxo
Me
2,4-diF—Ph
3-101
dioxo
nPr
2,4-diF—Ph
3-102
4-HM-dioxo
nPr
2,4-diF—Ph
3-103
4,5-diHM-dioxo
nPr
2,4-diF—Ph
3-104
4,5-diHE-dioxo
nPr
2,4-diF—Ph
3-105
dioxo
nBu
2,4-diF—Ph
3-106
4-HM-dioxo
nBu
2,4-diF—Ph
3-107
4,5-diHM-dioxo
nBu
2,4-diF—Ph
3-108
4,5-diHE-dioxo
nBu
2,4-diF—Ph
3-109
dioxo
iPr
2,4-diF—Ph
3-110
4-HM-dioxo
iPr
2,4-diF—Ph
3-111
4,5-diHM-dioxo
iPr
2,4-diF—Ph
3-112
4,5-diHE-dioxo
iPr
2,4-diF—Ph
3-113
dioxo
tBu
2,4-diF—Ph
3-114
4-HM-dioxo
tBu
2,4-diF—Ph
3-115
4,5-diHM-dioxo
tBu
2,4-diF—Ph
3-116
4,5-diHE-dioxo
tBu
2,4-diF—Ph
3-117
dioxo
CH2OAc
2,4-diF—Ph
3-118
4-HM-dioxo
CH2OAc
2,4-diF—Ph
3-119
4,5-diHM-dioxo
CH2OAc
2,4-diF—Ph
3-120
4,5-diHE-dioxo
CH2OAc
2,4-diF—Ph
3-121
dioxo
Me
2-Br-4-F—Ph
3-122
4-HM-dioxo
Me
2-Br-4-F—Ph
3-123
4,5-diHM-dioxo
Me
2-Br-4-F—Ph
3-124
4,5-diHE-dioxo
Me
2-Br-4-F—Ph
3-125
dioxo
nPr
2-Br-4-F—Ph
3-126
4-HM-dioxo
nPr
2-Br-4-F—Ph
3-127
4,5-diHM-dioxo
nPr
2-Br-4-F—Ph
3-128
4,5-diHE-dioxo
nPr
2-Br-4-F—Ph
3-129
dioxo
nBu
2-Br-4-F—Ph
3-130
4-HM-dioxo
nBu
2-Br-4-F—Ph
3-131
4,5-diHM-dioxo
nBu
2-Br-4-F—Ph
3-132
4,5-diHE-dioxo
nBu
2-Br-4-F—Ph
3-133
dioxo
iPr
2-Br-4-F—Ph
3-134
4-HM-dioxo
iPr
2-Br-4-F—Ph
3-135
4,5-diHM-dioxo
iPr
2-Br-4-F—Ph
3-136
4,5-diHE-dioxo
iPr
2-Br-4-F—Ph
3-137
dioxo
tBu
2-Br-4-F—Ph
3-138
4-IIM-dioxo
tBu
2-Br-4-F—Ph
3-139
4,5-diHM-dioxo
tBu
2-Br-4-F—Ph
3-140
4,5-diHE-dioxo
tBu
2-Br-4-F—Ph
3-141
dioxo
CH2OAc
2-Br-4-F—Ph
3-142
4-HM-dioxo
CH2OAc
2-Br-4-F—Ph
3-143
4,5-diHM-dioxo
CH2OAc
2-Br-4-F—Ph
3-144
4,5-diHE-dioxo
CH2OAc
2-Br-4-F—Ph
3-145
dioxo
Me
2-nBu-4-F—Ph
3-146
4-HM-dioxo
Me
2-nBu-4-F—Ph
3-147
4,5-diHM-dioxo
Me
2-nBu-4-F—Ph
3-148
4,5-diHE-dioxo
Me
2-nBu-4-F—Ph
3-149
dioxo
nPr
2-nBu-4-F—Ph
3-150
4-HM-dioxo
nPr
2-nBu-4-F—Ph
3-151
4,5-diHM-dioxo
nPr
2-nBu-4-F—Ph
3-152
4,5-diHE-dioxo
nPr
2-nBu-4-F—Ph
3-153
dioxo
nBu
2-nBu-4-F—Ph
3-154
4-HM-dioxo
nBu
2-nBu-4-F—Ph
3-155
4,5-diHM-dioxo
nBu
2-nBu-4-F—Ph
3-156
4,5-diHE-dioxo
nBu
2-nBu-4-F—Ph
3-157
dioxo
iPr
2-nBu-4-F—Ph
3-158
4-HM-dioxo
iPr
2-nBu-4-F—Ph
3-159
4,5-diHM-dioxo
iPr
2-nBu-4-F—Ph
3-160
4,5-diHE-dioxo
iPr
2-nBu-4-F—Ph
3-161
dioxo
tBu
2-nBu-4-F—Ph
3-162
4-HM-dioxo
tBu
2-nBu-4-F—Ph
3-163
4,5-diHM-dioxo
tBu
2-nBu-4-F—Ph
3-164
4,5-diHE-dioxo
tBu
2-nBu-4-F—Ph
3-165
dioxo
CH2OAc
2-nBu-4-F—Ph
3-166
4-HM-dioxo
CH2OAo
2-nBu-4-F—Ph
3-167
4,5-diHM-dioxo
CH2OAc
2-nBu-4-F—Ph
3-168
4,5-diHE-dioxo
CH2OAc
2-nBu-4-F—Ph
3-169
dioxo
Me
2-nPent-Ph
3-170
4-HM-dioxo
Me
2-nPent-Ph
3-171
4,5-diHM-dioxo
Me
2-nPent-Ph
3-172
4,5-diHE-dioxo
Me
2-nPent-Ph
3-173
dioxo
nPr
2-nPent-Ph
3-174
4-HM-dioxo
nPr
2-nPent-Ph
3-175
4,5-diHM-dioxo
nPr
2-nPent-Ph
3-176
4,5-diHE-dioxo
nPr
2-nPent-Ph
3-177
dioxo
nBu
2-nPent-Ph
3-178
4-HM-dioxo
nBu
2-nPent-Ph
3-179
4,5-diHM-dioxo
nBu
2-nPent-Ph
3-180
4,5-diHE-dioxo
nBu
2-nPent-Ph
3-181
dioxo
iPr
2-nPent-Ph
3-182
4-HM-dioxo
iPr
2-nPent-Ph
3-183
4,5-diHM-dioxo
iPr
2-nPent-Ph
3-184
4,5-diHE-dioxo
iPr
2-nPent-Ph
3-185
dioxo
tBu
2-nPent-Ph
3-186
4-HM-dioxo
tBu
2-nPent-Ph
3-187
4,5-diHM-dioxo
tBu
2-nPent-Ph
3-188
4,5-diHE-dioxo
tBu
2-nPent-Ph
3-189
dioxo
CH2OAc
2-nPent-Ph
3-190
4-HM-dioxo
CH2OAc
2-nPent-Ph
3-191
4,5-diHM-dioxo
CH2OAc
2-nPent-Ph
3-192
4,5-diHE-dioxo
CH2OAc
2-nPent-Ph
3-193
dioxo
Me
4-F-2-nPent-Ph
3-194
4-HM-dioxo
Me
4-F-2-nPent-Ph
3-195
4,5-diHM-dioxo
Me
4-F-2-nPent-Ph
3-196
4,5-diHE-dioxo
Me
4-F-2-nPent-Ph
3-197
dioxo
nPr
4-F-2-nPent-Ph
3-198
4-HM-dioxo
nPr
4-F-2-nPent-Ph
3-199
4,5-diHM-dioxo
nPr
4-F-2-nPent-Ph
3-200
4,5-diHE-dioxo
nPr
4-F-2-nPent-Ph
3-201
dioxo
nBu
4-F-2-nPent-Ph
3-202
4-HM-dioxo
nBu
4-F-2-nPent-Ph
3-203
4,5-diHM-dioxo
nBu
4-F-2-nPent-Ph
3-204
4,5-diHE-dioxo
nBu
4-F-2-nPent-Ph
3-205
dioxo
iPr
4-F-2-nPent-Ph
3-206
4-HM-dioxo
iPr
4-F-2-nPent-Ph
3-207
4,5-diHM-dioxo
iPr
4-F-2-nPent-Ph
3-208
4,5-diHE-dioxo
iPr
4-F-2-nPent-Ph
3-209
dioxo
tBu
4-F-2-nPent-Ph
3-210
4-HM-dioxo
tBu
4-F-2-nPent-Ph
3-211
4,5-diHM-dioxo
tBu
4-F-2-nPent-Ph
3-212
4,5-diHE-dioxo
tBu
4-F-2-nPent-Ph
3-213
dioxo
CH2OAc
4-F-2-nPent-Ph
3-214
4-HM-dioxo
CH2OAc
4-F-2-nPent-Ph
3-215
4,5-diHM-dioxo
CH2OAo
4-F-2-nPent-Ph
3-216
4,5-diHE-dioxo
CH2OAo
4-F-2-nPent-Ph
3-217
dioxo
Me
2-nHex—Ph
3-218
4-HM-dioxo
Me
2-nHex—Ph
3-219
4,5-diHM-dioxo
Me
2-nHex—Ph
3-220
4,5-diHE-dioxo
Me
2-nHex—Ph
3-221
dioxo
nPr
2-nHex—Ph
3-222
4-HM-dioxo
nPr
2-nHex—Ph
3-223
4,5-diHM-dioxo
nPr
2-nHex—Ph
3-224
4,5-diHE-dioxo
nPr
2-nHex—Ph
3-225
dioxo
nBu
2-nHex—Ph
3-226
4-HM-dioxo
nBu
2-nHex—Ph
3-227
4,5-diHM-dioxo
nBu
2-nHex—Ph
3-223
4,5-diHE-dioxo
nBu
2-nHex—Ph
3-229
dioxo
iPr
2-nHex—Ph
3-230
4-HM-dioxo
iPr
2-nHex—Ph
3-231
4,5-diHM-dioxo
iPr
2-nHex—Ph
3-232
4,5-diHE-dioxo
iPr
2-nHex—Ph
3-233
dioxo
tBu
2-nHex—Ph
3-234
4-HM-dioxo
tBu
2-nHex—Ph
3-235
4,5-diHM-dioxo
tBu
2-nHex—Ph
3-236
4,5-diHE-dioxo
tBu
2-nHex—Ph
3-237
dioxo
CH2OAc
2-nHex—Ph
3-238
4-HM-dioxo
CH2OAc
2-nHex—Ph
3-239
4,5-diHM-dioxo
CH2OAc
2-nHex—Ph
3-240
4,5-diHE-dioxo
CH2OAc
2-nHex—Ph
3-241
dioxo
Me
4-F-nHex—Ph
3-242
4-HM-dioxo
Me
4-F-nHex—Ph
3-243
4,5-diHM-dioxo
Me
4-F-nHex—Ph
3-244
4,5-diHE-dioxo
Me
4-F-nHex—Ph
3-245
dioxo
nPr
4-F-nHex—Ph
3-246
4-HM-dioxo
nPr
4-F-nHex—Ph
3-247
4,5-diHM-dioxo
nPr
4-F-nHex—Ph
3-248
4,5-diHE-dioxo
nPr
4-F-nHex—Ph
3-249
dioxo
nBu
4-F-nHex—Ph
3-250
4-HM-dioxo
nBu
4-F-nHex—Ph
3-251
4,5-diHM-dioxo
nBu
4-F-nHex—Ph
3-252
4,5-diHE-dioxo
nBu
4-F-nHex—Ph
3-253
dioxo
iPr
4-F-nHex—Ph
3-254
4-HM-dioxo
iPr
4-F-nHex—Ph
3-255
4,5-diHM-dioxo
iPr
4-F-nHex—Ph
3-256
4,5-diHE-dioxo
iPr
4-F-nHex—Ph
3-257
dioxo
tBu
4-F-nHex—Ph
3-258
4-HM-dioxo
tBu
4-F-nHex—Ph
3-259
4,5-diHM-dioxa
tBu
4-F-nHex—Ph
3-260
4,5-diHE-dioxo
tBu
4-F-nHex—Ph
3-261
dioxo
CH2OAc
4-F-nHex—Ph
3-262
4-HM-dioxo
CH2OAc
4-F-nHex—Ph
3-263
4,5-diHM-dioxo
CH2OAc
4-F-nHex—Ph
3-264
4,5-diHE-dioxo
CH2OAC
4-F-nHex—Ph
3-265
dioxo
Me
2-nHept-Ph
3-266
4-HM-dioxo
Me
2-nHept-Ph
3-267
4,5-diHM-dioxo
Me
2-nHept-Ph
3-268
4,5-diHE-dioxo
Me
2-nHept-Ph
3-269
dioxo
nPr
2-nHept-Ph
3-270
4-HM-dioxo
nPr
2-nHept-Ph
3-271
4,5-diHM-dioxo
nPr
2-nHept-Ph
3-272
4,5-diHE-dioxo
nPr
2-nHept-Ph
3-273
dioxo
nBu
2-nHept-Ph
3-274
4-HM-dioxo
nBu
2-nHept-Ph
3-275
4,5-diHM-dioxo
nBu
2-nHept-Ph
3-276
4,5-diHE-dioxo
nBu
2-nHept-Ph
3-277
dioxo
iPr
2-nHept-Ph
3-278
4-HM-dioxo
iPr
2-nHept-Ph
3-279
4,5-diHM-dioxo
iPr
2-nHept-Ph
3-280
4,5-diHE-dioxo
iPr
2-nHept-Ph
3-281
dioxo
tBu
2-nHept-Ph
3-282
4-HM-dioxo
tBu
2-nHept-Ph
3-283
4,5-diHM-dioxo
tBu
2-nHept-Ph
3-284
4,5-diHE-dioxo
tBu
2-nHept-Ph
3-285
dioxo
CH2OAc
2-nHept-Ph
3-286
4-HM-dioxo
CH2OAc
2-nHept-Ph
3-287
4,5-diHM-dioxo
CH2OAc
2-nHept-Ph
3-288
4,5-diHE-dioxo
CH2OAc
2-nHept-Ph
3-289
dioxo
Me
4-F-2-nHept-Ph
3-290
4-HM-dioxo
Me
4-F-2-nHept-Ph
3-291
4,5-diHM-dioxo
Me
4-F-2-nHept-Ph
3-292
4,5-diHE-dioxo
Me
4-F-2-nHept-Ph
3-293
dioxo
nPr
4-F-2-nHept-Ph
3-294
4-HM-dioxo
nPr
4-F-2-nHept-Ph
3-295
4,5-diHM-dioxo
nPr
4-F-2-nHept-Ph
3-296
4,5-diHE-dioxo
nPr
4-F-2-nHept-Ph
3-297
dioxo
nBu
4-F-2-nHept-Ph
3-298
4-HM-dioxo
nBu
4-F-2-nHept-Ph
3-299
4,5-diHM-dioxo
nBu
4-F-2-nHept-Ph
3-300
4,5-diHE-dioxo
nBu
4-F-2-nHept-Ph
3-301
dioxo
iPr
4-F-2-nHept-Ph
3-302
4-HM-dioxo
iPr
4-F-2-nHept-Ph
3-303
4,5-diHM-dioxo
iPr
4-F-2-nHept-Ph
3-304
4,5-diHE-dioxo
iPr
4-F-2-nHept-Ph
3-305
dioxo
tBu
4-F-2-nHept-Ph
3-306
4-HM-dioxo
tBu
4-F-2-nHept-Ph
3-307
4,5-diHM-dioxo
tBu
4-F-2-nHept-Ph
3-308
4,5-diHE-dioxo
tBu
4-F-2-nHept-Ph
3-309
dioxo
CH2OAc
4-F-2-nHept-Ph
3-310
4-HM-dioxo
CH2OAc
4-F-2-nHept-Ph
3-311
4,5-diHM-dioxo
CH2OAc
4-F-2-nHept-Ph
3-312
4,5-diHE-dioxo
CH2OAc
4-F-2-nHept-Ph
3-313
dioxo
Me
2-nOct-Ph
3-314
4-HM-dioxo
Me
2-nOct-Ph
3-315
4,5-diHM-dioxo
Me
2-nOct-Ph
3-316
4,5-diHE-dioxo
Me
2-nOct-Ph
3-317
dioxo
nPr
2-nOct-Ph
3-318
4-HM-dioxo
nPr
2-nOct-Ph
3-319
4,5-diHM-dioxo
nPr
2-nOct-Ph
3-320
4,5-diHE-dioxo
nPr
2-nOct-Ph
3-321
dioxo
nBu
2-nOct-Ph
3-322
4-HM-dioxo
nBu
2-nOct-Ph
3-323
4,5-diHM-dioxo
nBu
2-nOct-Ph
3-324
4,5-diHE-dioxo
nBu
2-nOct-Ph
3-325
dioxo
iPr
2-nOct-Ph
3-326
4-HM-dioxo
iPr
2-nOct-Ph
3-327
4,5-diHM-dioxo
iPr
2-nOct-Ph
3-328
4,5-diHE-dioxo
iPr
2-nOct-Ph
3-329
dioxo
tBu
2-nOct-Ph
3-330
4-HM-dioxo
tBu
2-nOct-Ph
3-331
4,5-diHM-dioxo
tBu
2-nOct-Ph
3-332
4,5-diHE-dioxo
tBu
2-nOct-Ph
3-333
dioxo
CH2OAo
2-nOct-Ph
3-334
4-HM-dioxo
CH2OAc
2-nOct-Ph
3-335
4,5-diHM-dioxo
CH2OAc
2-nOct-Ph
3-336
4,5-diHE-dioxo
CH2OAc
2-nOct-Ph
3-337
dioxo
Me
4-F-2-nOct-Ph
3-338
4-HM-dioxo
Me
4-F-2-nOct-Ph
3-339
4,5-diHM-dioxo
Me
4-F-2-nOct-Ph
3-340
4,5-diHE-dioxo
Me
4-F-2-nOct-Ph
3-341
dioxo
nPr
4-F-2-nOct-Ph
3-342
4-HM-dioxo
nPr
4-F-2-nOct-Ph
3-343
4,5-diHM-dioxo
nPr
4-F-2-nOct-Ph
3-344
4,5-diHE-dioxo
nPr
4-F-2-nOct-Ph
3-345
dioxo
nBu
4-F-2-nOct-Ph
3-346
4-HM-dioxo
nBu
4-F-2-nOct-Ph
3-347
4,5-diHM-dioxo
nBu
4-F-2-nOct-Ph
3-348
4,5-diHE-dioxo
nBu
4-F-2-nOct-Ph
3-349
dioxo
iPr
4-F-2-nOct-Ph
3-350
4-HM-dioxo
iPr
4-F-2-nOct-Ph
3-351
4,5-diHM-dioxo
iPr
4-F-2-nOct-Ph
3-352
4,5-diHE-dioxo
iPr
4-F-2-nOct-Ph
3-353
dioxo
tBu
4-F-2-nOct-Ph
3-354
4-HM-dioxo
tBu
4-F-2-nOct-Ph
3-355
4,5-diHM-dioxo
tBu
4-F-2-nOct-Ph
3-356
4,5-diHE-dioxo
tBu
4-F-2-nOct-Ph
3-357
dioxo
CH2OAc
4-F-2-nOct-Ph
3-358
4-HM-dioxo
CH2OAc
4-F-2-nOct-Ph
3-359
4,5-diHM-dioxo
CH2OAc
4-F-2-nOct-Ph
3-360
4,5-diHE-dioxo
CH2OAc
4-F-2-nOct-Ph
3-361
dioxo
Me
Ph
3-362
4-HM-dioxo
Me
Ph
3-363
4,5-diHM-dioxo
Me
Ph
3-364
4,5-diHE-dioxo
Me
Ph
3-365
dioxo
nPr
Ph
3-366
4-HM-dioxo
nPr
Ph
3-367
4,5-diHM-dioxo
nPr
Ph
3-368
4,5-diHE-dioxo
nPr
Ph
3-369
dioxo
nBu
Ph
3-370
4-HM-dioxo
nBu
Ph
3-371
4,5-diHM-dioxo
nBu
Ph
3-372
4,5-diHE-dioxo
nBu
Ph
3-373
dioxo
iPr
Ph
3-374
4-HM-dioxo
iPr
Ph
3-375
4,5-diHM-dioxo
iPr
Ph
3-376
4,5-diHE-dioxo
iPr
Ph
3-377
dioxo
tBu
Ph
3-378
4-HM-dioxo
tBu
Ph
3-379
4,5-diHM-dioxo
tBu
Ph
3-380
4,5-diHE-dioxo
tBu
Ph
3-381
dioxo
CH2OAc
Ph
3-382
4-HM-dioxo
CH2OAc
Ph
3-383
4,5-diHM-dioxo
CH2OAc
Ph
3-384
4,5-diHE-dioxo
CH2OAc
Ph
3-385
dioxo
Me
4-F—Ph
3-386
4-HM-dioxo
Me
4-F—Ph
3-387
4,5-diHM-dioxo
Me
4-F—Ph
3-388
4,5-diHE-dioxo
Me
4-F—Ph
3-389
dioxo
nPr
4-F—Ph
3-390
4-HM-dioxo
nPr
4-F—Ph
3-391
4.5-diHM-dioxo
nPr
4-F—Ph
3-392
4,5-diHE-dioxo
nPr
4-F—Ph
3-393
dioxo
nBu
4-F—Ph
3-394
4-HM-dioxo
nBu
4-F—Ph
3-395
4,5-diHM-dioxo
nBu
4-F—Ph
3-396
4,5-diHE-dioxo
nBu
4-F—Ph
3-397
dioxo
iPr
4-F—Ph
3-398
4-HM-dioxo
iPr
4-F—Ph
3-399
4,5-diHM-dioxo
iPr
4-F—Ph
3-400
4,5-diHE-dioxo
iPr
4-F—Ph
3-401
dioxo
tBu
4-F—Ph
3-402
4-HM-dioxo
tBu
4-F—Ph
3-403
4,5-diHM-dioxo
tBu
4-F—Ph
3-404
4,5-diHE-dioxo
tBu
4-F—Ph
3-405
dioxo
CH2OAc
4-F—Ph
3-406
4-HM-dioxo
CH2OAc
4-F—Ph
3-407
4,5-diHM-dioxo
CH2OAc
4-F—Ph
3-408
4,5-diHE-dioxo
CH2OAc
4-F—Ph
3-409
dioxo
Me
2-Cl-4-Me—Ph
3-410
4-HM-dioxo
Me
2-Cl-4-Me—Ph
3-411
4,5-diHM-dioxo
Me
2-Cl-4-Me—Ph
3-412
4,5-diHE-dioxo
Me
2-Cl-4-Me—Ph
3-413
dioxo
nPr
2-Cl-4-Me—Ph
3-414
4-HM-dioxo
nPr
2-Cl-4-Me—Ph
3-415
4,5-diHM-dioxo
nPr
2-Cl-4-Me—Ph
3-416
4,5-diHE-dioxo
nPr
2-Cl-4-Me—Ph
3-417
dioxo
nBu
2-Cl-4-Me—Ph
3-418
4-HM-dioxo
nBu
2-Cl-4-Me—Ph
3-419
4,5-diHM-dioxo
nBu
2-Cl-4-Me—Ph
3-420
4,5-diHE-dioxo
nBu
2-Cl-4-Me—Ph
3-421
dioxo
iPr
2-Cl-4-Me—Ph
3-422
4-HM-dioxo
iPr
2-Cl-4-Me—Ph
3-423
4,5-diHM-dioxo
iPr
2-Cl-4-Me—Ph
3-424
4,5-diHE-dioxo
iPr
2-Cl-4-Me—Ph
3-425
dioxo
tBu
2-Cl-4-Me—Ph
3-426
4-HM-dioxo
tBu
2-Cl-4-Me—Ph
3-427
4,5-diHM-dioxo
tBu
2-Cl-4-Me—Ph
3-428
4,5-diHE-dioxo
tBu
2-Cl-4-Me—Ph
3-429
dioxo
CH2OAc
2-Cl-4-Me—Ph
3-430
4-HM-dioxo
CH2OAc
2-Cl-4-Me—Ph
3-431
4,5-diHM-dioxo
CH2OAc
2-Cl-4-Me—Ph
3-432
4,5-diHE-dioxo
CH2OAc
2-Cl-4-Me—Ph
3-433
dioxo
Me
2-nBu—Ph
3-434
4-HM-dioxo
Me
2-nBu—Ph
3-435
4,5-diHM-dioxo
Me
2-nBu—Ph
3-436
4,5-diHE-dioxo
Me
2-nBu—Ph
3-437
dioxo
nPr
2-nBu—Ph
3-438
4-HM-dioxo
nPr
2-nBu—Ph
3-439
4,5-diHM-dioxo
nPr
2-nBu—Ph
3-440
4,5-diHE-dioxo
nPr
2-nBu—Ph
3-441
dioxo
nBu
2-nBu—Ph
3-442
4-HM-dioxo
nBu
2-nBu—Ph
3-443
4,5-diHM-dioxo
nBu
2-nBu—Ph
3-444
4,5-diHE-dioxo
nBu
2-nBu—Ph
3-445
dioxo
iPr
2-nBu—Ph
3-446
4-HM-dioxo
iPr
2-nBu—Ph
3-447
4,5-diHM-dioxo
iPr
2-nBu—Ph
3-448
4,5-diHE-dioxo
iPr
2-nBu—Ph
3-449
dioxo
tBu
2-nBu—Ph
3-450
4-HM-dioxo
tBu
2-nBu—Ph
3-451
4,5-diHM-dioxo
tBu
2-nBu—Ph
3-452
4,5-diHE-dioxo
tBu
2-nBu—Ph
3-453
dioxo
CH2OAc
2-nBu—Ph
3-454
4-HM-dioxo
CH2OAc
2-nBu—Ph
3-455
4,5-diHM-dioxo
CH2OAc
2-nBu—Ph
3-456
4,5-diHE-dioxo
CH2OAc
2-nBu—Ph
3-457
dioxo
Me
2-nPr—Ph
3-458
4-HM-dioxo
Me
2-nPr—Ph
3-459
4,5-diHM-dioxo
Me
2-nPr—Ph
3-460
4,5-diHE-dioxo
Me
2-nPr—Ph
3-461
dioxo
nPr
2-nPr—Ph
3-462
4-HM-dioxo
nPr
2-nPr—Ph
3-463
4,5-diHM-dioxo
nPr
2-nPr—Ph
3-464
4,5-diHE-dioxo
nPr
2-nPr—Ph
3-465
dioxo
nBu
2-nPr—Ph
3-466
4-HM-dioxo
nBu
2-nPr—Ph
3-467
4.5-diHM-dioxo
nBu
2-nPr—Ph
3-468
4,5-diHE-dioxo
nBu
2-nPr—Ph
3-469
dioxo
iPr
2-nPr—Ph
3-470
4-HM-dioxo
iPr
2-nPr—Ph
3-471
4,5-diHM-dioxo
iPr
2-nPr—Ph
3-472
4,5-diHE-dioxo
iPr
2-nPr—Ph
3-473
dioxo
tBu
2-nPr—Ph
3-474
4-HM-dioxo
tBu
2-nPr—Ph
3-475
4,5-diHM-dioxo
tBu
2-nPr—Ph
3-476
4,5-diHE-dioxo
tBu
2-nPr—Ph
3-477
dioxo
CH2OAc
2-nPr—Ph
3-478
4-HM-dioxo
CH2OAc
2-nPr—Ph
3-479
4,5-diHM-dioxo
CH2OAc
2-nPr—Ph
3-480
4,5-diHE-dioxo
CH2OAc
2-nPr—Ph
3-481
dioxo
Me
4-F-2-nPr—Ph
3-482
4-HM-dioxo
Me
4-F-2-nPr—Ph
3-483
4,5-diHM-dioxo
Me
4-F-2-nPr—Ph
3-484
4,5-diHE-dioxo
Me
4-F-2-nPr—Ph
3-485
dioxo
nPr
4-F-2-nPr—Ph
3-486
4-HM-dioxo
nPr
4-F-2-nPr—Ph
3-487
4,5-diHM-dioxo
nPr
4-F-2-nPr—Ph
3-488
4,5-diHE-dioxo
nPr
4-F-2-nPr—Ph
3-489
dioxo
nBu
4-F-2-nPr—Ph
3-490
4-HM-dioxo
nBu
4-F-2-nPr—Ph
3-491
4,5-diHM-dioxo
nBu
4-F-2-nPr—Ph
3-492
4,5-diHE-dioxo
nBu
4-F-2-nPr—Ph
3-493
dioxo
iPr
4-F-2-nPr—Ph
3-494
4-HM-dioxo
iPr
4-F-2-nPr—Ph
3-495
4,5-diHM-dioxo
iPr
4-F-2-nPr—Ph
3-496
4,5-diHE-dioxo
iPr
4-F-2-nPr—Ph
3-497
dioxo
tBu
4-F-2-nPr—Ph
3-498
4-HM-dioxo
tBu
4-F-2-nPr—Ph
3-499
4,5-diHM-dioxo
tBu
4-F-2-nPr—Ph
3-500
4,5-diHE-dioxo
tBu
4-F-2-nPr—Ph
3-501
dioxo
CH2OAc
4-F-2-nPr—Ph
3-502
4-HM-dioxo
CH2OAc
4-F-2-nPr—Ph
3-503
4,5-diHM-dioxo
CH2OAc
4-F-2-nPr—Ph
3-504
4,5-diHE-dioxo
CH2OAc
4-F-2-nPr—Ph
In the compounds having the general formula (I) of the present invention, as preferred compounds exemplified compound Nos.: 1-12, 1-13, 1-19, 1-20, 1-26, 1-28, 1-30, 1-32, 1-34, 1-36, 1-38, 1-40, 1-42, 1-44, 1-46, 1-48, 1-50, 1-54, 1-58, 1-60, 1-62, 1-66, 1-68, 1-70, 1-72, 1-74, 1-78, 1-80, 1-82, 1-86, 1-100, 1-101, 1-107, 1-108, 1-114, 1-116, 1-118, 1-120, 1-122, 1-124, 1-126, 1-128, 1-130, 1-132, 1-134, 1-136, 1-138, 1-142, 1-146, 1-148, 1-150, 1-154, 1-156, 1-158, 1-160, 1-162, 1-166, 1-168, 1-170, 1-174, 1-188, 1-189, 1-195, 1-196, 1-202, 1-204, 1-206, 1-208, 1-210, 1-212, 1-214, 1-216, 1-218, 1-220, 1-222, 1-224, 1-226, 1-230, 1-234, 1-236, 1-238, 1-242, 1-244, 1-246, 1-248, 1-250, 1-254, 1-256, 1-258, 1-262, 1-276, 1-277, 1-283, 1-284, 1-290, 1-292, 1-294, 1-296, 1-298, 1-300, 1-302, 1-304, 1-306, 1-308, 1-310, 1-312, 1-314, 1-318, 1-322, 1-324, 1-326, 1-330, 1-332, 1-334, 1-336, 1-338, 1-342, 1-344, 1-346, 1-350, 1-353, 1-355, 1-360 to 1-369, 1-371, 1-372, 1-378, 1-380, 1-382, 1-384, 1-386, 1-388, 1-390, 1-392, 1-394, 1-396, 1-398, 1-400, 1-402, 1-406, 1-410, 1-412, 1-414, 1-418, 1-420, 1-422, 1-424, 1-426, 1-430, 1-432, 1-434, 1-438, 1-452, 1-453, 1-459, 1-460, 1-466, 1-468, 1-470, 1-472, 1-474, 1-476, 1-478, 1-480, 1-482, 1-484, 1-486, 1-488, 1-490, 1-494, 1-498, 1-500, 1-502, 1-506, 1-508, 1-510, 1-512, 1-514, 1-518, 1-520, 1-522, 1-526, 1-540, 1-541, 1-547, 1-548, 1-554, 1-556, 1-558, 1-560, 1-562, 1-564, 1-566, 1-568, 1-570, 1-572, 1-574, 1-576, 1-578, 1-582, 1-586, 1-588, 1-590, 1-594, 1-596, 1-598, 1-600, 1-602, 1-604, 1-606, 1-608, 1-610, 1-614, 1-628, 1-629, 1-635, 1-636, 1-642, 1-644, 1-646, 1-648, 1-650, 1-652, 1-654, 1-656, 1-658, 1-660, 1-662, 1-664, 1-666, 1-670, 1-674, 1-676, 1-678, 1-682, 1-684, 1-686, 1-688, 1-690, 1-694, 1-696, 1-698, 1-702, 1-712 to 1-720, 1-723, 1-724, 1-730, 1-732, 1-734, 1-736, 1-738, 1-740, 1-742, 1-744, 1-746, 1-748, 1-750, 1-752, 1-754, 1-758, 1-762, 1-764, 1-766, 1-770, 1-772, 1-774, 1-776, 1-778, 1-782, 1-784, 1-786, 1-790, 1-804, 1-805, 1-811, 1-812, 1-818, 1-820, 1-822, 1-824, 1-826, 1-828, 1-830, 1-832, 1-834, 1-836, 1-838, 1-840, 1-842, 1-846, 1-850, 1-852, 1-854, 1-858, 1-860, 1-862, 1-864, 1-866, 1-870, 1-872, 1-874, 1-878, 1-888 to 1-896, 1-899, 1-900, 1-906, 1-908, 1-910, 1-912, 1-914, 1-916, 1-918, 1-920, 1-922, 1-924, 1-926, 1-928, 1-930, 1-934, 1-938, 1-940, 1-942, 1-946, 1-948, 1-950, 1-952, 1-954, 1-958, 1-960, 1-962, 1-966, 1-980, 1-981, 1-987, 1-988, 1-994, 1-996, 1-998, 1-1000, 1-1002, 1-1004, 1-1006, 1-1008, 1-1010, 1-1012, 1-1014, 1-1016, 1-1018, 1-1022, 1-1026, 1-1028, 1-1030, 1-1034, 1-1036, 1-1038, 1-1040, 1-1042, 1-1046, 1-1048, 1-1050, 1-1054, 1-1057, 1-1062, 1-1063, 1-1066, 1-1067 to 1-1070, 1-1074, 1-1079, 1-1080, 1-1083, 1-1085 to 1-1087, 1-1091, 1-1096, 1-1097, 1-1100, 1-1102 to 1-1104, 1-1108, 1-1113, 1-1114, 1-1117, 1-1119 to 1-1121, 1-1125, 1-1130, 1-1131, 1-1134, 1-1136 to 1-1138, 1-1142, 1-1147, 1-1148, 1-1151, 1-1153 to 1-1155, 1-1159, 1-1164, 1-1165, 1-1168, 1-1170 to 1-1172, 1-1176, 1-1181, 1-1182, 1-1185, 1-1187 to 1-1189, 1-1193, 1-1198, 1-1199, 1-1202, 1-1204 to 1-1206, 1-1210, 1-1215, 1-1216, 1-1219, 1-1221 to 1-1223, 1-1227, 1-1232, 1-1233, 1-1236, 1-1238 to 1-1240, 1-1244, 1-1249, 1-1250, 1-1253, 1-1255 to 1-1257, 1-1261, 1-1266, 1-1267, 1-1270, 1-1272 to 1-1274, 1-1278, 1-1283, 1-1284, 1-1287, 1-1289 to 1-1291, 1-1295, 1-1300, 1-1301, 1-1304, 1-1306 to 1-1308, 1-1312, 1-1317, 1-1318, 1-1321, 1-1323 to 1-1325, 1-1329, 1-1334, 1-1335, 1-1337, 1-1340 to 1-1342, 1-1346, 1-1351, 1-1352, 1-1355, 1-1357 to 1-1359, 1-1374, 1-1375, 1-1381, 1-1382, 1-1388, 1-1390, 1-1392, 1-1394, 1-1396, 1-1398, 1-1400, 1-1402, 1-1404, 1-1406, 1-1408, 1-1410, 1-1412, 1-1416, 1-1420, 1-1422, 1-1428, 1-1430, 1-1432, 1-1434, 1-1436, 1-1440, 1-1442, 1-1444, 1-1448, 1-1462, 1-1463, 1-1469, 1-1470, 1-1476, 1-1478, 1-1480, 1-1482, 1-1484, 1-1486, 1-1488, 1-1490, 1-1492, 1-1494, 1-1496, 1-1498, 1-1500, 1-1504, 1-1508, 1-1510, 1-1516, 1-1518, 1-1520, 1-1522, 1-1524, 1-1528, 1-1530, 1-1532, 1-1536, 1-1550, 1-1551, 1-1557, 1-1558, 1-1564, 1-1566, 1-1568, 1-1570, 1-1572, 1-1574, 1-1576, 1-1578, 1-1580, 1-1582, 1-1584, 1-1586, 1-1588, 1-1592, 1-1596, 1-1598, 1-1604, 1-1606, 1-1608, 1-1610, 1-1612, 1-1616, 1-1618, 1-1620, 1-1624, 1-1638, 1-1639, 1-1645, 1-1646, 1-1652, 1-1654, 1-1656, 1-1658, 1-1660, 1-1662, 1-1664, 1-1666, 1-1668, 1-1670, 1-1672, 1-1674, 1-1676, 1-1680, 1-1684, 1-1686, 1-1692, 1-1694, 1-1696, 1-1698, 1-1700, 1-1704, 1-1706, 1-1708, 1-1712, 1-1726, 1-1727, 1-1733, 1-1734, 1-1740, 1-1742, 1-1744, 1-1746, 1-1748, 1-1750, 1-1752, 1-1754, 1-1756, 1-1758, 1-1760, 1-1762, 1-1764, 1-1768, 1-1772, 1-1774, 1-1780, 1-1782, 1-1784, 1-1786, 1-1788, 1-1792, 1-1794, 1-1796, 1-1800, 1-1814, 1-1815, 1-1821, 1-1822, 1-1828, 1-1830, 1-1832, 1-1834, 1-1836, 1-1838, 1-1840, 1-1842, 1-1844, 1-1846, 1-1848, 1-1850, 1-1852, 1-1856, 1-1860, 1-1862, 1-1868, 1-1870, 1-1872, 1-1874, 1-1876, 1-1880, 1-1882, 1-1884, 1-1888, 1-1902, 1-1903, 1-1909, 1-1910, 1-1916, 1-1918, 1-1920, 1-1922, 1-1924, 1-1926, 1-1928, 1-1930, 1-1932, 1-1934, 1-1936, 1-1938, 1-1940, 1-1944, 1-1948, 1-1950, 1-1956, 1-1958, 1-1960, 1-1962, 1-1964, 1-1968, 1-1970, 1-1972, 1-1976, 1-1989, 1-1990, 1-1996, 1-1997, 1-2003, 1-2005, 1-2007, 1-2009, 1-2011, 1-2013, 1-2015, 1-2017, 1-2019, 1-2021, 1-2023, 1-2025, 1-2027, 1-2031, 1-2035, 1-2037, 1-2043, 1-2045, 1-2047, 1-2049, 1-2051, 1-2055, 1-2057, 1-2059, 1-2063, 1-2077, 1-2078, 1-2084, 1-2085, 1-2091, 1-2093, 1-2095, 1-2097, 1-2099, 1-2101, 1-2103, 1-2105, 1-2107, 1-2109, 1-2111, 1-2113, 1-2115, 1-2119, 1-2123, 1-2125, 1-2131, 1-2133, 1-2135, 1-2137, 1-2139, 1-2143, 1-2145, 1-2147, 1-2151, 1-2154, 1-2157, 1-2160, 1-2163, 1-2166, 1-2169, 1-2172, 1-2175, 1-2178, 1-2181, 1-2184, 1-2187, 1-2190, 1-2193, 1-2196, 1-2199, 1-2202, 1-2205, 1-2208, 1-2211, 1-2214, 1-2217 to 1-2221, 1-2224 to 1-2228, 1-2231 to 1-2235, 1-2238 to 1-2242, 1-2245 to 1-2249, 1-2252 to 1-2256, 1-2259 to 1-2263, 1-2266 to 1-2270, 1-2273 to 1-2277, 1-2280 to 1-2284, 1-2287 to 1-2291, 1-2294 to 1-2298, 1-2301 to 1-2305, 1-2308 to 1-2312, 1-2315 to 1-2319, 1-2322 to 1-2326, 1-2329 to 1-2333, 1-2336 to 1-2340, 1-2343 to 1-2347, 1-2350 to 1-2354, 1-2357 to 1-2361, 1-2364 to 1-2368, 1-2371 to 1-2375, 1-2378 to 1-2382, 1-2385 to 1-2389, 1-2392 to 1-2396, 1-2399 to 1-2403, 1-2406 to 1-2410, 1-2413 to 1-2417, 1-2420 to 1-2424, 1-2427 to 1-2431, 1-2434 to 1-2438, 1-2441 to 1-2445, 1-2448 to 1-2452, 1-2455 to 1-2459, 1-2462 to 1-2466, 1-2469 to 1-2473, 1-2476 to 1-2480, 1-2483 to 1-2487, 1-2490 to 1-2494, 1-2497 to 1-2501, 1-2504 to 1-2508, 1-2511 to 1-2515, 1-2518 to 1-2522, 1-2525 to 1-2529, 1-2532 to 1-2536, 1-2539 to 1-2543, 1-2546 to 1-2550, 1-2553 to 1-2557, 1-2560 to 1-2564, 1-2567 to 1-2571, 1-2574 to 1-2578, 1-2581 to 1-2585, 1-2588 to 1-2592, 1-2595 to 1-2599, 1-2602 to 1-2606, 1-2609 to 1-2613, 1-2616 to 1-2620, 1-2623 to 1-2627, 2-3, 2-4, 2-7, 2-8, 2-11, 2-12, 2-15, 2-16, 2-19, 2-20, 2-23, 2-24, 2-27, 2-28, 2-31, 2-32, 2-35, 2-36, 2-39, 2-40, 2-43, 2-44, 2-47, 2-48, 2-51, 2-52, 2-59, 2-60, 2-83, 2-84, 3-3, 3-4, 3-7, 3-8, 3-11, 3-12, 3-15, 3-16, 3-27, 3-28, 3-31, 3-32, 3-35, 3-36, 3-39, 3-40, 3-51, 3-52, 3-55, 3-56, 3-59, 3-60, 3-63, 3-64, 3-75, 3-76, 3-79, 3-80, 3-83, 3-84, 3-87, 3-88, 3-99, 3-100, 3-103, 3-104, 3-107, 3-108, 3-111, 3-112, 3-123, 3-124, 3-127, 3-128, 3-131, 3-132, 3-135, 3-136, 3-147, 3-148, 3-151, 3-152, 3-155, 3-156, 3-159, 3-160, 3-171, 3-172, 3-175, 3-176, 3-179, 3-180, 3-183, 3-184, 3-195, 3-196, 3-199, 3-200, 3-203, 3-204, 3-207, 3-208, 3-219, 3-220, 3-223, 3-224, 3-227, 3-228, 3-231, 3-232, 3-243, 3-244, 3-247, 3-248, 3-251, 3-252, 3-255, 3-256, 3-267, 3-268, 3-271, 3-272, 3-275, 3-276, 3-279, 3-280, 3-291, 3-292, 3-295, 3-296, 3-299, 3-300, 3-303, 3-304, 3-339, 3-340, 3-343, 3-344, 3-347, 3-348, 3-351, 3-352, 3-483, 3-484, 3-487, 3-488, 3-491, 3-492, 3-495, and 3-496 can be mentioned,
more preferably, exemplified compound Nos.: 1-12, 1-26, 1-30, 1-34, 1-38, 1-42, 1-46, 1-58, 1-66, 1-70, 1-78, 1-100, 1-114, 1-118, 1-122, 1-126, 1-130, 1-134, 1-146, 1-154, 1-158, 1-166, 1-188, 1-202, 1-206, 1-210, 1-214, 1-218, 1-222, 1-234, 1-242, 1-246, 1-254, 1-276, 1-290, 1-294, 1-298, 1-302, 1-306, 1-310, 1-322, 1-330, 1-334, 1-342, 1-364, 1-378, 1-382, 1-386, 1-390, 1-394, 1-398, 1-410, 1-418, 1-422, 1-430, 1-452, 1-466, 1-470, 1-474, 1-478, 1-482, 1-486, 1-498, 1-506, 1-510, 1-518, 1-540, 1-554, 1-558, 1-562, 1-566, 1-570, 1-574, 1-586, 1-594, 1-598, 1-604, 1-606, 1-628, 1-642, 1-646, 1-650, 1-654, 1-658, 1-662, 1-674, 1-682, 1-686, 1-694, 1-716, 1-730, 1-734, 1-738, 1-742, 1-746, 1-750, 1-762, 1-770, 1-774, 1-782, 1-804, 1-818, 1-822, 1-826, 1-830, 1-834, 1-838, 1-850, 1-858, 1-862, 1-870, 1-892, 1-906, 1-910, 1-914, 1-918, 1-922, 1-926, 1-938, 1-946, 1-950, 1-958, 1-980, 1-994, 1-998, 1-1002, 1-1006, 1-1010, 1-1014, 1-1026, 1-1034, 1-1038, 1-1046, 1-1227, 1-1232, 1-1239, 1-1240, 1-1244, 1-1249, 1-1256, 1-1257, 1-1261, 1-1266, 1-1273, 1-1274, 1-1278, 1-1283, 1-1290, 1-1291, 1-1295, 1-1300, 1-1307, 1-1308, 1-1374, 1-1388, 1-1392, 1-1396, 1-1400, 1-1404, 1-1408, 1-1420, 1-1428, 1-1432, 1-1440, 1-1462, 1-1476, 1-1480, 1-1484, 1-1488, 1-1492, 1-1496, 1-1508, 1-1516, 1-1520, 1-1528, 1-1550, 1-1564, 1-1568, 1-1572, 1-1576, 1-1580, 1-1584, 1-1596, 1-1604, 1-1608, 1-1616, 1-1638, 1-1652, 1-1656, 1-1660, 1-1664, 1-1668, 1-1672, 1-1684, 1-1692, 1-1696, 1-1704, 1-1726, 1-1740, 1-1744, 1-1748, 1-1752, 1-1756, 1-1760, 1-1772, 1-1780, 1-1784, 1-1792, 1-1814, 1-1828, 1-1832, 1-1836, 1-1840, 1-1844, 1-1848, 1-1860, 1-1868, 1-1872, 1-1880, 1-1902, 1-1916, 1-1920, 1-1924, 1-1928, 1-1932, 1-1936, 1-1948, 1-1956, 1-1960, 1-1968, 1-1989, 1-2003, 1-2007, 1-2011, 1-2015, 1-2019, 1-2023, 1-2035, 1-2043, 1-2047, 1-2055, 1-2077, 1-2091, 1-2095, 1-2099, 1-2103, 1-2107, 1-2111, 1-2123, 1-2131, 1-2135, 1-2143, 1-2219, 1-2220, 1-2226, 1-2227, 1-2233, 1-2234, 1-2240, 1-2241, 1-2247, 1-2248, 1-2254, 1-2255, 1-2261, 1-2262, 1-2268, 1-2269, 1-2275, 1-2276, 1-2282, 1-2283, 1-2289, 1-2290, 1-2296, 1-2297, 1-2303, 1-2304, 1-2310, 1-2311, 1-2317, 1-2318, 1-2324, 1-2325, 1-2331, 1-2332, 1-2338, 1-2339, 1-2345, 1-2346, 1-2352, 1-2353, 1-2359, 1-2360, 1-2366, 1-2367, 1-2373, 1-2374, 1-2380, 1-2381, 1-2387, 1-2388, 1-2394, 1-2395, 1-2401, 1-2402, 1-2408, 1-2409, 1-2415, 1-2416, 1-2422, 1-2423, 1-2429, 1-2430, 1-2436, 1-2437, 1-2443, 1-2444, 1-2450, 1-2451, 1-2457, 1-2458, 1-2464, 1-2465, 1-2471, 1-2472, 1-2478, 1-2479, 1-2485, 1-2486, 1-2492, 1-2493, 1-2499, 1-2500, 1-2506, 1-2507, 1-2513, 1-2514, 1-2520, 1-2521, 1-2527, 1-2528, 1-2534, 1-2535, 1-2541, 1-2542, 1-2548, 1-2549, 1-2555, 1-2556, 1-2562, 1-2563, 1-2569, 1-2570, 1-2576, 1-2577, 1-2583, 1-2584, 1-2590, 1-2591, 1-2597, 1-2598, 1-2604, 1-2605, 1-2611, 1-2612, 1-2618, 1-2619, 1-2625, 1-2626, 2-3, 2-7, 2-11, 2-15, 2-19, 2-23, 2-27, 2-31, 2-35, 2-39, 2-43, 2-47, 2-51, 2-59, 2-83, 3-7, 3-31, 3-55, 3-79, 3-103, 3-127, 3-151, 3-175, 3-199, 3-223, 3-247, 3-271, 3-295, 3-343 and 3-487can be mentioned,
even more preferably,
The compound having the general formula (I) according to the present invention can easily be prepared in accordance with Method A to Method C shown hereafter.
Method A is a method to prepare a compound having the general formula (I), by introducing a cyclic ketal in the initial stage of the preparation.
Method B is a method to prepare a compound having the general formula (I), by introducing a cyclic ketal in the final stage of the preparation.
Method C is a method to prepare a compound having the general formula (I), by introducing R5 in the final stage of the preparation.
##STR00012##
In the aforementioned Method A to Method C, ring A, ring B, X, Y, R1, R2, R3, R5, m and n have the same meanings as defined above, L represents a leaving group and Z represents a protective group.
In the reactions of Method A to Method C, in the case where the compound as the reactive substrate has a group such as an amino group, hydroxy group and/or carboxyl group, which inhibits the intended reaction, these groups may be protected with a protective group as necessary. The protective group of a group which inhibits the intended reaction is not limited so long as it is a protective group which is ordinarily used to conduct the reaction, and may be, for example, a protective w group described in “Protective Groups in Organic Synthesis, 3rd edition, T. W. Greene & P. G. M. Wuts; John Wiley & Sons, Inc.”
A protective group of an amino group can be used without particular limitation so long as it is a group generally used as a protective group of an amino group, and preferably, formyl, the aforementioned C1-C6 alkylcarbonyl group; the aforementioned arylcarbonyl group; the aforementioned C1-C6 alkoxycarbonyl group; the aforementioned C1-C6 alkanoyl group which is substituted with halogen; aralkyl groups such as benzyl, phenethyl, 3-phenylpropyl, 4-phenylbutyl, α-naphthylmethyl, β-naphthylmethyl, diphenylmethyl, triphenylmethyl, α-naphthyldiphenylmethyl or 9-anthrylmethyl; the aforementioned aralkyloxycarbonyl group and the like can be mentioned.
A protective group of a hydroxy group can be used without particular limitation so long as it is a group generally used as a protective group of a hydroxy group, and preferably, formyl, C1-C6 alkylcarbonyl groups such as acetyl, arylcarbonyls such as benzoyl group; and alkoxylated alkoxymethyls such as 2-methoxyethoxymethyl can be mentioned.
A protective group of a carboxyl group can be used without particular limitation so long as it is a group generally used as a protective group of a carboxyl group, and preferably, the aforementioned C1-C6 alkyl group; and aralkyl groups such as benzyl, phenethyl and phenylpropyl can be mentioned.
Further, these protective groups of groups which inhibit the intended reaction may be cleaved as necessary. The cleavage reaction of these protective groups, which is the desired reaction, may be conducted in accordance with conventional procedures which are used in the field of synthetic organic chemistry (for example, the procedure described in the aforementioned Protective Groups in Organic Synthesis, 3rd edition, T. W. Greene & P. G. M. Wuts; John Wiley & Sons, Inc).
<Method A>
Step 1 of Method A is a step to react a ketone compound (1) with a compound (2) or a compound (3), which is compound (2) having its terminal substituted with a trimethylsilyl group (described as TMS in the aforementioned scheme), in an inert solvent in the presence of acid, to prepare a cyclic ketal compound (4).
This step can adopt a cyclic ketalation reaction (protection) of a ketone, which is widely used in general organic synthesis, and can be conducted in accordance with the procedure described in T. W. Greene, P. C. Wuts, Protective Groups in organic Synthesis. Third Edition, 1999, Chapter 4, pp. 293-368, John Wiley & Sons, Inc. and the like, or in accordance with similar procedures.
Here, the cyclic ketal compound (4) can also be prepared by the following procedure (Step 1′ of Method A).
Step 1′ of Method A is a step to react a dimethylketal compound (5) with compound (2) or compound (3), in an inert solvent in the presence of acid, to prepare a cyclic ketal compound (4). This reaction can be conducted in accordance with the same procedure as or based on the procedure of Step 1.
Step 2 of Method A is a step to allow the cyclic ketal compound (4) obtained by Step 1 or Step 1′ to undergo a Dieckmann reaction, to prepare a ketoester compound (7).
This step can adopt a Dieckmann reaction which is widely used generally in organic synthesis, and can be conducted in accordance with the procedure described in Chemical Pharmaceutical Bulletin (Chem. Pharm. Bull.) Vol. 29, pp. 3238-3248 (1981) and the like, or based on that procedure.
Here, the ketoester compound (7) can also be prepared by the following procedure (Step 2′ of Method A).
Step 2′ of Method A is a step to react a ketone compound (6) with a dialkyl carbonate, in an inert solvent in the presence of base, to prepare a ketoester compound (7).
This step can adopt an ester group introducing reaction which is widely used generally in organic synthesis, and can be conducted in accordance with the procedure described in Canadian Journal of Chemistry (Can. J. Chem.) Vol. 70, pp. 1406-1426 (1992) and the like, or based on that procedure.
Step 3 of Method A is a step to enolate the ketoester compound (7) obtained in Step 2 or Step 2′, in an inert solvent in the presence of base, to prepare a compound (8) having a leaving group L.
This step can be conducted in accordance with the procedure described in Journal of American Chemical Society (J. Am. Chem. Soc.), Vol. 120, pp. 3664-3670 (1998) and the like, or based on that procedure.
“Leaving group” in the definition of L generally represents a group which leaves as a nucleophilic residue, and for example, halogen atoms such as a fluorine atom, chlorine atom, bromine atom and iodine atom; lower alkanesulfonyloxy groups such as methanesulfonyloxy and ethanesulfonyloxy; halogeno lower alkanesulfonyloxy groups such as trifluoromethanesulfonyloxy and pentafluoroethanesulfonyloxy; and arylsulfonyloxy groups such as benzenesulfonyloxy, p-toluenesulfonyloxy and p-nitrobenzenesulfonyloxy can be mentioned. Preferably, it is a halogeno lower alkanesulfonyloxy group, particularly preferably a trifluoromethanesulfonyloxy group.
The inert solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some degree, and for example, aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethyleneglycoldimethyl ether; amides such as formamide, N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone and hexamethylphosphorotriamide; or a solvent mixture of these can be mentioned. Preferably, it is a halogenated hydrocarbon, more preferably dichloromethane.
The base used includes inorganic bases such as alkali metal carbonates such as sodium carbonate, potassium carbonate and lithium carbonate; alkali metal hydrogen carbonates such as sodium hydrogen carbonate, potassium hydrogen carbonate and lithium hydrogen carbonate; alkali metal hydrides such as lithium hydride, sodium hydride and potassium hydride; alkali metal fluorides such as sodium fluoride and potassium fluoride; organic bases such as alkali metal alkoxides such as sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium t-butoxide and lithium methoxide; N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4-(N,N-dimethylamino)pyridine, 2,6-di(t-butyl)-4-methylpyridine, quinoline, N,N-dimethylaniline, N,N-diethylaniline, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), 1,4-diazabicyclo[2.2.2]octane (DABCO) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), preferably alkali metal hydrides or organic bases, and more preferably sodium hydride or diisopropylethylamine.
Reaction temperature varies depending on the starting compound and reaction reagent, and the reaction is conducted from −100° C. to 100° C., preferably from −78° C. to 50° C.
Reaction time varies depending on the reaction temperature, starting compound, reaction reagent or the type of solvent used, and it is generally in the range from 1 minute to 48 hours, preferably from 5 minutes to 12 hours.
Step 4 of Method A is a step to react the compound (8) having a leaving group L obtained in Step 3 with a thiol compound (9) in an inert solvent in the presence of a base, to prepare compound (10).
“Protective group” of the sulfanyl group in the definition of Z is not particularly limited so long as it is a protective group of a sulfanyl group which is widely used generally in organic synthesis, and alkanoyl groups such as formyl, acetyl, propionyl and butyryl, and arylcarbonyl groups such as benzoyl, α-naphthoyl, β-naphthoyl, pyridoyl, thienoyl and furoyl can be mentioned, for example. Preferably, it is a group which forms a pharmacologically acceptable ester, and is more preferably an acetyl group.
The inert solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some degree, and for example, aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethyleneglycoldimethyl ether; aprotic polar solvents such as formamide, N,N-dimethylformamide, N,N-dimethylacetamide and dimethyl sulfoxide; or a solvent mixture of these can be mentioned. Preferably, it is an aprotic polar solvent, more preferably N,N-dimethylformamide.
The base used includes inorganic bases such as alkali metal carbonates, e.g. sodium carbonate, potassium carbonate and lithium carbonate; alkali metal hydrogen carbonates such as sodium hydrogen carbonate, potassium hydrogen carbonate and lithium hydrogen carbonate; alkali metal hydrides such as lithium hydride, sodium hydride and potassium hydride; alkali metal fluorides such as sodium fluoride and potassium fluoride; organic bases such as alkali metal alkoxides, e.g. sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium t-butoxide and lithium methoxide; N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4-(N,N-dimethylamino)pyridine, 2,6-di(t-butyl)-4-methylpyridine, quinoline, N,N-dimethylaniline, N,N-diethylaniline, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), 1,4-diazabicyclo[2.2.2]octane (DABCO) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) can be mentioned, and is preferably an alkali metal hydride, more preferably sodium hydride or potassium hydride.
Reaction temperature varies depending on the starting compound and reaction reagent, and the reaction is conducted from −78° C. to 100° C., preferably from −20° C. to 50° C.
Reaction time varies depending on the reaction temperature, starting compound, reaction reagent or the type of solvent used, and it is generally in the range from 1 minute to 120 hours, preferably from 10 minutes to 72 hours.
Step 5 of Method A is a step to deprotect the protective group of the sulfanyl group of the compound (10) obtained in Step 4, in an inert solvent, to prepare compound (11).
This step is a deprotection step of a protective group of a sulfanyl group which is widely used in general organic synthesis, and is conducted in accordance with the procedure described in the aforementioned “Protective Groups in Organic Synthesis, 3rd edition, T. W. Greene & P. G. M. Wuts; John Wiley & Sons, Inc.” and the like, or based on that procedure, and can be preferably conducted by a deprotection procedure in an inert solvent in the presence of base.
The inert solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some degree, and for example, aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethyleneglycoldimethyl ether; alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, t-butanol, isoamyl alcohol, diethylene glycol, glycerin, octanol, cyclohexanol and 2-methoxyethanol; amides such as formamide, N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone and hexamethylphosphortriamide; sulfoxides such as dimethyl sulfoxide and sulfolane; or a solvent mixture of these can be mentioned, and is preferably an alcohol, and more preferably methanol or ethanol.
The base used includes alkali metal carbonates such as sodium carbonate, potassium carbonate and lithium carbonate; alkali metal hydrogen carbonates such as sodium hydrogencarbonate, potassium hydrogencarbonate and lithium hydrogencarbonate; organic bases such as alkali metal alkoxides, e.g. sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium t-butoxide and lithium methoxide; N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4-(N,N-dimethylamino)pyridine, 2,6-di(t-butyl)-4-methylpyridine, quinoline, N,N-dimethylaniline, N,N-diethylaniline, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), 1,4-diazabicyclo[2.2.2]octane (DABCO) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), preferably alkali metal carbonates, and more preferably potassium carbonate.
Reaction temperature varies depending on the starting compound and reaction reagent, and the reaction is conducted from −78° C. to 100° C., preferably from −20° C. to 50° C.
Reaction time varies depending on the reaction temperature, starting compound, reaction reagent or the type of solvent used, and it is generally from 1 minute to 24 hours, preferably from 5 minutes to 5 hours.
Step 6 of Method A is a step to chlorosulfonylate the thiol group of the compound (11) obtained in Step 5, in an inert solvent, to prepare compound (12).
This step can be conducted in accordance with the procedure described in Journal of Organic Chemistry (J. Org. Chem.), Vol. 16, pp. 621-625 (1951) and the like, or based on that procedure.
The inert solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some degree, and for example, aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride and dichloroethane; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethyleneglycoldimethyl ether; alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, t-butanol, isoamyl alcohol, diethylene glycol, glycerin, octanol, cyclohexanol and 2-methoxyethanol; aprotic polar solvents such as N, N-dimethylformamide, N,N-dimethylacetamide and dimethyl sulfoxide; nitrites such as acetonitrile; esters such as methyl acetate and ethyl acetate; carboxylic acids such as formic acid, acetic acid, propionic acid and trifluoroacetic acid; water; or a solvent mixture of these can be mentioned. Preferably, it is a solvent mixture of carboxylic acids and water or a solvent mixture of nitrites and water, more preferably a solvent mixture of acetic acid and water, or a solvent mixture of acetonitrile and water.
Reaction temperature varies according to the starting compound and reaction reagent, and the reaction is conducted from −78° C. to 100° C., preferably from −20° C. to 50° C.
Reaction time varies depending on the reaction temperature, starting compound, reaction reagent or the type of solvent used, and it is generally from 1 minute to 12 hours, preferably from 5 minutes to 1 hour.
Step 7 of Method A is a step to react the compound (12) obtained in Step 6 with an amine compound (13) in an inert solvent in the presence or absence of base, to prepare a compound of general formula (I).
The inert solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some degree, and for example, aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride and dichloroethane; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethyleneglycoldimethyl ether; aprotic polar solvents such as N,N-dimethylformamide, N,N-dimethylacetamide and dimethyl sulfoxide; nitrites such as acetonitrile; esters such as methyl acetate and ethyl acetate; or a solvent mixture of these can be mentioned. Preferably, it is an ester, more preferably ethyl acetate.
The base used includes alkali metal hydrates such as lithium hydrate, sodium hydrate and potassium hydrate; organic bases such as N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4-(N,N-dimethylamino)pyridine, 2,6-di(t-butyl)-4-methylpyridine, quinoline, N,N-dimethylaniline, N,N-diethylaniline, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), 1,4-diazabicyclo[2.2.2]octane (DABCO) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), preferably organic bases, and more preferably triethylamine.
Reaction temperature varies depending on the starting compound and reaction reagent, and the reaction is conducted from −78° C. to 100° C., preferably from −20° C. to 50° C.
Reaction time varies depending on the reaction temperature, starting compound, reaction reagent or the type of solvent used, and it is generally in the range from 1 minute to 120 hours, preferably from 10 minutes to 48 hours.
<Method B>
Step 8 of Method B is a step to hydrolyze the cyclic ketal compound (14) obtained in Method A in an inert solvent in the presence of acid, to prepare a ketone compound (15).
This step can adopt a deprotection reaction of a cyclic ketal compound which is widely used generally in organic synthesis, and can be conducted in accordance with the procedure described in the aforementioned T. W. Greene, O. G. Wuts, Protective Groups in Organic Synthesis. Third Edition, 1999, Chapter 4, pp. 293-368, John Wiley & Sons, Inc. and the like, or based on that procedure.
Step 9 of Method B is a step to prepare a dimethylketal compound (16) with the ketone compound (15) obtained in Step 8 in an inert solvent in the presence of acid.
This step can adopt a dimethylketalation reaction (protection) of a ketone which is widely used generally in organic synthesis, and can be conducted in accordance with the procedure described in the aforementioned T. W. Greene, 0. G. Wuts, Protective Groups in Organic Synthesis. Third Edition, 1999, Chapter 4, pp. 293-368, John Wiley & Sons, Inc. and the like, or based on that procedure.
Step 10 of Method B is a step to react the ketone compound (15) obtained in Step 8 with the compound (2) or compound (3) in an inert solvent in the presence of acid, to prepare a compound having the general formula (I).
Here, this reaction can be conducted in accordance with a similar procedure to Step 1.
Step 10′ of Method B is a step to react the dimethylketal compound (16) obtained in Step 9 with the compound (2) or compound (3) in an inert solvent in the presence of acid, to prepare a compound having the general formula (I).
Here, this reaction can be conducted in accordance with a similar procedure to Step 1′.
<Method C>
Step 11 of Method C is a step, in the case where R5 of the cyclic ketal compound (14) obtained in Method A or the compound having the general formula (I) obtained in Method B is a hydrogen atom, to react it with R5-L (17) in an inert solvent in the presence of base, to prepare a compound having the general formula (I) which is substituted with a desired R5.
R5 and L represent the same meanings as described above, and “leaving group” in the definition of L represents a group which leaves as a nucleophilic residue, and for example, halogen atoms such as a fluorine atom, chlorine atom, bromine atom and iodine atom; lower-alkane sulfonyloxy groups such as methanesulfonyloxy and ethanesulfonyloxy; halogeno lower alkanesulfonyloxy groups such as trifluoromethanesulfonyloxy and pentafluoroethanesulfonyloxy; arylsulfonyloxy groups such as benzenesulfonyloxy, p-toluenesulfonyloxy and p-nitrobenzenesulfonyloxy; can be mentioned. Preferably, it is a halogen atom, particularly preferably an iodine atom.
The inert solvent used is not particularly limited so long as it does not inhibit the reaction and dissolves the starting material to some degree, and includes, for example, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone and cyclohexanone; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran and dioxane; aprotic polar solvents such as dimethylformamide, dimethylacetamide and dimethyl sulfoxide; nitrites such as acetonitrile; esters such as methyl acetate and ethyl acetate; aromatic hydrocarbons such as benzene, toluene and xylene; aliphatic hydrocarbons such as pentane, hexane and heptane, preferably, ethers, ketones or aprotic polar solvents, and more preferably, tetrahydrofuran, acetone or dimethylformamide.
The base used includes alkali metal carbonates such as sodium carbonate, potassium carbonate and lithium carbonate; alkali metal hydrogen carbonates such as sodium hydrogen carbonate, potassium hydrogen carbonate and lithium hydrogen carbonate; organic bases such as alkali metal alkoxides such as sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium t-butoxide and lithium methoxide; N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4-(N,N-dimethylamino)pyridine, 2,6-di(t-butyl)-4-methylpyridine, quinoline, N,N-dimethylaniline, N,N-diethylaniline, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), 1,4-diazabicyclo[2.2.2]octane (DABCO) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), preferably alkali metal carbonates, and more preferably potassium carbonate.
Reaction temperature varies depending on the starting compound and reaction reagent, and the reaction is conducted from −78° C. to 150° C., preferably from −20° C. to 100° C.
Reaction time varies depending on the reaction temperature, starting compound, reaction reagent or the type of solvent used, and it is generally in the range from 1 minute to 24 hours, preferably from 10 minutes to 5 hours.
After each of the aforementioned reactions is completed, the desired compound is collected from the reaction mixture in accordance with general procedures.
For example, the reaction mixture is neutralized as needed, and after filtration to remove insoluble matters in the case where insoluble matters exist, the reaction solution is extracted with an organic solvent such as ethyl acetate, which does not blend with water. Then after washing the reaction solution with water and the like, the organic layer containing the desired compound is separated and dried over anhydrous magnesium sulfate and the like, and then the solvent is evaporated to give the desired compound.
The obtained desired compound may, if necessary, be separated and purified by ordinary procedures such as recrystallization and reprecipitation, or by a procedure generally used for separation and purification of organic compounds such as appropriately combining an adsorption column chromatography method which uses silica gel, alumina or florisil of magnesium-silica type as a support; a method using a synthetic adsorbent agent such as distribution column chromatography which uses Sephadex LH-20 (produced by Pharmacia), Amberlite XAD-11 (produced by Rohm and Haas) or Diaion HP-20 (produced by Mitsubishi Chemical Corporation) as a support, a method using ion exchange chromatography, or normal phase or reverse phase column chromatography by silica gel or alkylated silica gel (preferably high performance liquid chromatography) and eluting with an appropriate eluent.
The starting compounds such as (1), (2), (3), (5), (6), (9), (13) and (17) as reactive substances of the present invention are publicly known or can easily be prepared in accordance with publicly known procedures.
The compound having the general formula (I) according to the present invention or pharmacologically acceptable salts thereof possesses excellent activity to suppress intracellular signal transduction or cell activation in various cells such as monocytes, macrophages and vascular endothelial cells, the intracellular signal transduction and cell activation being induced by endotoxin, and to suppress various cell responses induced by the intracellular signal transduction and cell activation such as an excess generation of inflammatory mediators such as TNF-α. Therefore, it is useful as a medicament, especially as a prophylactic and/or therapeutic agent for various diseases which are associated with intracellular signal transduction or cell activation induced by endotoxin, and with various cell responses (for example, excess generation of inflammatory mediators such as TNF-α) which are induced by the intracellular signal transduction and cell activation. As for such medicament, a prophylactic and/or therapeutic agent for ischemic brain disorder, arteriosclerosis, poor prognosis after coronary angioplasty, heart failure, diabetes, diabetic complication, joint inflammation, osteoporosis, osteopenia, sepsis, autoimmune disease, tissue disorder and rejection after organ transplantation, bacterial infection, virus infection, gastritis, pancreatitis, nephritis, pneumonia, hepatitis or leukemia can be mentioned.
In the case where the compound having the general formula (I) according to the present invention or the pharmacologically acceptable salts thereof is used as a prophylactic agent or a therapeutic agent for the aforementioned diseases, it can be mixed with excipients, diluents and the like that are themselves pharmacologically acceptable, and administered orally as a tablet, capsule, granules, powder or syrup, or administrated parenterally as an injection for subcutaneous injection, intramuscular injection or intravenous injection or as a suppository.
These pharmaceutical preparations are prepared in accordance with known processes by using additives including excipients (for example, organic excipients such as sugar derivatives, e.g. lactose, sucrose, glucose, mannitol or sorbitol; starch derivatives, e.g. corn starch, potato starch, α-starch or dextrin; cellulose derivatives, e.g. crystalline cellulose; gum arabic; dextran; or pullulan, and inorganic excipients such as silicate derivatives, e.g. light silicic anhydride, synthetic aluminum silicate, calcium silicate, metamagnesium aluminate; phosphates, e.g. calcium hydrogenphosphate; carbonates, e.g. calcium carbonate; salts of sulfuric acid such as calcium sulfate, can be mentioned), lubricants (for example, stearic acid, stearic acid metal salts such as calcium stearate or magnesium stearate; talc; colloid silica; waxes such as bees wax or spermaceti, boric acid; adipic acid; sulfates such as sodium sulfate; glycol; fumaric acid; sodium benzoate; DL leucine; lauryl sulfates such as sodium lauryl sulfate or magnesium lauryl sulfate; silicic acids such as silicic anhydride or silicate hydrate; and the aforementioned starch derivatives can be mentioned), binders (for example, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, polyvinylpyrrolidone, macrogol and compounds similar to the aforementioned excipient can be mentioned), disintegrants (for example, cellulose derivatives such as low-substituted hydroxypropyl cellulose, carboxymethyl cellulose, calcium carboxymethyl cellulose or internally crosslinked sodium carboxymethyl cellulose; or chemically modified starches or celluloses such as carboxymethyl starch, sodium carboxymethyl starch or crosslinked polyvinylpyrrolidone can be mentioned), emulsifiers (for example, colloidal clays such as bentonite or bee gum; metal hydroxides such as magnesium hydroxide or aluminum hydroxide; anionic surfactants such as sodium lauryl sulfate or calcium stearate; cationic surfactants such as benzalkonium chloride; and nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene sorbitan fatty acid ester or sucrose fatty acid ester), stabilizers (for example, paraoxybenzoic acid esters such as methyl paraben or propyl paraben; alcohols such as chlorobutanol, benzyl alcohol or phenyl ethyl alcohol, benzalkonium chloride; phenols such as phenol or cresol; thimerosal; dehydroacetic acid; and sorbic acid can be mentioned) and corrigents (for example, commonly used sweeteners, acidifiers or fragrances can be mentioned) or diluents.
The amount of dosage varies according to symptoms and age, and it is desirable that the compound of the present invention is administered orally or parenterally to an adult human within a lower limit of 0.01 mg/kg (preferably 0.10 mg/kg) and an upper limit of 1000 mg/kg (preferably 100 mg/kg) per day, once a day or several times in parts depending on the symptoms.
Hereinafter, the present invention will be described in detail with reference to Examples and Test Examples, however, the scope of the present invention is not limited to these.
##STR00013##
19.97 g (55.4 mmol) of ethyl 8-trifluoromethanesulfonyloxy-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate [compound described as compound 6 in Tetrahedron Letter, Vol. 39, pp. 6139-6142 (1998)] was dissolved in 200 ml of dimethylformamide, and 9.50 g (83.1 mmol) of potassium thioacetate was added thereto with stirring under ice-cooling, followed by stirring at room temperature for 91 hours. To the reaction solution was added ice water and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=17:3) to give 7.15 g of the title compound as a pale brown oil (yield: 45%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.20 (2H, q, 7 Hz), 4.04-3.96 (4H, m), 2.73-2.66 (4H, m), 2.34 (3H, s), 1.87 (2H, t, J=6 Hz), 1.28 (3H, t, J=7 Hz).
7.14 g (24.9 mmol) of ethyl 8-acetylsulfanyl-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (1a) was dissolved in 145 ml of methanol, and 2.58 g (18.7 mmol) of potassium carbonate was added thereto with stirring under ice-cooling, followed by stirring at the same temperature for 1 hour and then at room temperature for 1 hour. The reaction solution was made acidic by addition of 1N hydrochloric acid and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=9:1) to give 5.63 g of the title compound as a pale yellow oil (yield: 92%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.32 (1H, s), 4.21 (2H, q, 7 Hz), 4.04-3.95 (4H, m), 2.72-2.67 (2H, m), 2.59-2.57 (2H, m), 1.82 (2H, t, J=7 Hz), 1.30 (3H, t, J=7 Hz).
To a saturated solution prepared by blowing chlorine gas into 80 ml of solution mixture of acetonitrile-water (1:1) for 20 minutes was added a solution of 5.00 g (20.5 mmol) of ethyl 8-mercapto-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (1b) in 10 ml of acetonitrile with stirring under ice-cooling. Chlorine gas was further blown into the reaction solution for 10 minutes at the same temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 5.83 g of the title compound as a colorless oil (yield: 92%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.30 (2H, q, 7 Hz), 4.05-3.98 (4H, m), 2.91-2.86 (2H, m), 2.71-2.69 (2H, m), 1.93 (2H, t, J=7 Hz), 1.34 (3H, t, J=7 Hz).
To a solution of 197 mg (1.35 mmol) of 2-chloro-4-fluoroaniline and 0.20 ml (1.42 mmol) of triethylamine in 5 ml of ethyl acetate was added dropwise a solution of 400 mg (1.29 mmol) of ethyl 8-chlorosulfonyl-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (1c) in 3 ml of ethyl acetate with stirring under ice-cooling, followed by stirring at room temperature for 48 hours. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1), and the resulting solid was further washed with a mixed solution of hexane-isopropyl ether (1:1) to give 325 mg of the title compound as a white powder (yield: 60%).
Melting point 117-119° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.67 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.98 (2H, m), 6.83 (1H, s), 4.43-4.41 (1H, m), 4.26-4.01 (5H, m), 3.95-3.88 (1H, m), 2.56-2.45 (2H, m), 2.24-2.11 (1H, m), 1.88-1.80 (1H, m), 1.27 (3H, t, J=7 Hz).
##STR00014##
Following the process described in Example (1d), aniline was used in place of 2-chloro-4-fluoroaniline to give the title compound as an amorphous substance (yield: 81%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.37-7.31 (4H, m), 7.21-7.15 (1H, m), 6.95 (1H, s), 6.85-6.87 (1H, m), 4.30-4.20 (3H, m), 4.13-4.01 (3H, m), 3.94-3.88 (1H, m), 2.48-2.41 (1H, m), 2.31 (1H, td, J=14 Hz, 3 Hz), 2.10-2.00 (1H, m), 1.86-1.80 (1H, m), 1.31 (3H, t, J=7 Hz).
##STR00015##
Following the process described in Example (1d), 2-butylaniline was used in place of 2-chloro-4-fluoroaniline to give the title compound as a colorless oil (56% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.55-7.52 (1H, m), 7.22-7.17 (2H, m), 7.13-7.08 (1H, m), 6.85-6.84 (1H, m), 6.63 (1H, s), 4.47-4.44 (1H, m), 4.25-4.02 (5H, m), 3.95-3.89 (1H, m), 2.71-2.62 (2H, m), 2.54-2.38 (2H, m), 2.19-2.09 (1H, m), 1.86-1.81 (1H, m), 1.62-1.53 (2H, m), 1.45-1.34 (2H, m), 1.26 (3H, t, J=7 Hz), 0.95 (3H, t, J=7 Hz).
##STR00016##
Following the process described in Example (1d), 2-hexylaniline was used in place of 2-chloro-4-fluoroaniline to give the title compound as a pale yellow oil (82% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.55-7.52 (1H, m), 7.22-7.17 (2H, m), 7.13-7.08 (1H, m), 6.85-6.84 (1H, m), 6.63 (1H, s), 4.47-4.44 (1H, m), 4.25-4.02 (5H, m), 3.95-3.89 (1H, m), 2.70-2.61 (2H, m), 2.54-2.38 (2H, m), 2.19-2.09 (1H, m), 1.86-1.81 (1H, m), 1.64-1.54 (2H, m), 1.41-1.24 (6H, m), 1.26 (3H, t, J=7 Hz), 0.91-0.85 (3H, m).
##STR00017##
Following the process described in Example (1d), 2-heptylaniline was used in place of 2-chloro-4-fluoroaniline to give the title compound as a pale yellow oil (87% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.55-7.52 (1H, m), 7.22-7.17 (2H, m), 7.13-7.08 (1H, m), 6.85-6.84 (1H, m), 6.63 (1H, s), 4.47-4.44 (1H, m), 4.25-4.02 (5H, m), 3.95-3.89 (1H, m), 2.69-2.61 (2H, m), 2.54-2.38 (2H, m), 2.19-2.09 (1H, m), 1.86-1.81 (1H, m), 1.64-1.54 (2H, m), 1.42-1.23 (8H, m), 1.26 (3H, t, J=7 Hz), 0.88 (3H, t, J=7 Hz).
##STR00018##
Following the process described in Example (id), 1H-pyrrol-1-ylamine was used in place of 2-chloro-4-fluoroaniline to give the title compound as a white powder (yield: 33%).
Melting point: 115-117° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 8.05 (1H, s), 6.99 (2H, t, J=2 Hz), 6.94 (1H, s), 6.17 (2H, t, J=2 Hz), 4.55-4.51 (1H, m), 4.30 (2H, q, J=7 Hz), 4.14-4.03 (3H, m), 3.98-3.89 (1H, m), 2.51-2.44 (1H, m), 2.26-2.05 (2H, m), 1.89-1.83 (1H, m), 1.35 (3H, t, J=7 Hz).
##STR00019##
To 2.55 g (6.07 mmol) of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 1 was added 100 ml of a mixed solution of 1N hydrochloric acid-tetrahydrofuran (1:1), and the reaction solution was stirred at room temperature for 64 hours. Tetrahydrofuran was distilled off under reduced pressure, the residue was extracted by addition of ethyl acetate, and the organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=4:1), to give 2.19 g of the title compound as a pale brown powder (yield: 96%).
Melting point: 128-130° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.69 (1H, dd, J=9 Hz, 5 Hz), 7.20 (1H, dd, J=8 Hz, 3 Hz), 7.09-7.03 (1H, m), 6.91 (2H, s), 4.68 (1H, dd, J=5 Hz, 2 Hz), 4.28-4.18 (2H, m), 3.21-3.09 (1H, m), 2.80-2.72 (1H, m), 2.57-2.49 (1H, m), 2.44-2.31 (1H, m), 1.28 (3H, t, J=7 Hz).
##STR00020##
100 mg (0.27 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3-oxo-1-cyclohexene-1-carboxylate obtained in Example 7 was dissolved in 2 ml of toluene, and 0.04 ml (0.54 mmol) of propane-1,3-diol and 68 mg (0.27 mmol) of pyridinium p-toluenesulfonate were added thereto, followed by heating under reflux for 1 hour. After the reaction solution was cooled to room temperature, a saturated aqueous sodium hydrogencarbonate solution was added and extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1), and the resulting solid was further washed with hexane to give 60 mg of the title compound as a white powder (yield: 51%).
Melting point: 120-121° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.36 (1H, s), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.01 (1H, dd, J=7 Hz, 2 Hz), 6.98 (1H, s), 4.45-4.39 (1H, m), 4.27-4.12 (2H, m), 4.11-3.84 (4H, m), 2.46-2.06 (4H, m), 1.92-1.67 (2H, m), 1.28 (3H, t, J=7 Hz).
##STR00021##
Following the process described in Example 8, 2,2-dimethylpropane-1,3-diol was used in place of propane-1,3-diol to give the title compound as a pale brown oil (yield: 64%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.64 (1H, dd, J=9 Hz, 5 Hz), 7.31 (1H, s), 7.13 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.94 (2H, m), 4.45-4.39 (1H, m), 4.27-4.12 (2H, m), 3.69-3.46 (4H, m), 2.42-2.11 (4H, m), 1.28 (3H, t, J=7 Hz), 1.03 (3H, s), 0.97 (3H, s).
##STR00022##
100 mg (0.27 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3-oxo-1-cyclohexene-1-carboxylate obtained in Example 7 was dissolved in 1 ml of dichloromethane and 0.034 ml (0.405 mmol) of ethane-1,2-dithiol and 0.025 ml (0.203 mmol) of boron trifluoride diethyl etherate were added thereto with stirring under ice-cooling, followed by stirring at room temperature for 1 hour. To the reaction solution was added a 1N aqueous sodium hydroxide solution and the mixture was extracted with diethyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The resulting solid was washed with diethyl ether and then with hexane to give 325 mg of the title compound as a white powder (76% yield).
Melting point: 160-161° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.10 (1H, s), 7.04-6.96 (2H, m), 4.40 (1H, d, J=5 Hz), 4.25-4.10 (2H, m), 3.52-3.26 (4H, m), 2.82-2.72 (1H, m), 2.58-2.50 (1H, m), 2.33-2.24 (1H, m), 2.11-1.99 (1H, m), 1.27 (3H, t, J=7 Hz).
##STR00023##
Following the process described in Example 10, propane-1,3-dithiol was used in place of ethane-1,2-dithiol to give the title compound as an amorphous substance (72% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.40 (1H, s), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.03-6.96 (1H, m), 6.94 (1H, s), 4.51 (1H, d, J=5 Hz), 4.24-4.11 (2H, m), 3.17-3.07 (1H, m), 2.98-2.77 (3H, m), 2.61-2.51 (1H, m), 2.47-2.38 (1H, m), 2.36-2.27 (1H, m), 2.25-2.13 (1H, m), 2.12-1.95 (2H, m), 1.27 (3H, t, J=7 Hz).
##STR00024##
Following the process described in Example 10, 2-mercapteothanol was used in place of ethane-1,2-dithiol to give the title compound as a white powder (61% yield).
Melting point: 133-134° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.06 (0.4H, s), 7.04-6.96 (2.6H, m), 4.46 (0.4H, dd, J=5 Hz, 3 Hz), 4.39-4.01 (4.6H, m), 3.23-3.06 (2H, m), 2.77-2.51 (1.6H, m), 2.45-2.36 (0.4H, m), 2.20-2.00 (2H, m), 1.27 (3H, t, J=7 Hz).
##STR00025##
80 mg (0.18 mmol) of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dithiaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 10 was dissolved in 2 ml of dichloromethane, 91 mg (1.08 mmol) of sodium hydrogencarbonate was added thereto and subsequently 239 mg (0.90 mmol) of m-chloroperbenzoic acid (65%) was added with stirring under ice-cooling, followed by stirring at room temperature for 5 hours. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel thin layer chromatography (solvent; hexane:ethyl acetate=1:1) to give 42 mg of the title compound as a white powder (yield: 45%).
Melting point: 88-90° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.15 (1H, dd, J=8 Hz, 3 Hz), 7.06-6.98 (2H, m), 6.92 (1H, s), 4.57 (1H, d, J=5 Hz), 4.26-4.16 (2H, m), 3.79-3.60 (4H, m), 3.14-2.98 (1H, m), 2.69-2.60 (1H, m), 2.45-2.36 (1H, m), 2.29-2.16 (1H, m), 1.28 (3H, t, J=7 Hz).
##STR00026##
50 mg (0.133 mmol) of ethyl 6-[1-(2-chloro-4-fluorophenyl)sulfamoyl]-3-oxo-1-cyclohexene-1-carboxylate obtained in Example 7 and 0.01 ml (0.146 mmol) of dibromomethane were dissolved in 1 ml of tetrahydrofuran, and 0.18 ml (0.279 mmol) of n-butyllithium/hexane solution (1.58 M) was added dropwise thereto at −78° C., followed by stirring at room temperature for 4 hours. After the reaction solution was cooled with ice, a saturated aqueous ammonium chloride solution was added and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel thin layer chromatography (solvent; hexane:ethyl acetate=2:1) to give 7 mg of the title compound as a yellow oil (yield: 14%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.68 (1H, dd, J=9 Hz, 5 Hz), 7.15 (1H, dd, J=8 Hz, 3 Hz), 7.07-6.91 (2H, m), 6.60 (1H, s), 4.50 (1H, d, J=4 Hz), 4.27-4.06 (2H, m), 2.98-2.92 (1H, m), 2.91-2.88 (1H, m), 2.83-2.70 (1H, m), 2.68-2.59 (1H, m), 2.21-2.07 (2H, m), 1.25 (3H, t, J=7 Hz).
##STR00027##
100 mg (0.27 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3-oxo-1-cyclohexene-1-carboxylate obtained in Example 7 and 69 mg (0.35 mmol) of (R)-2,3-dihydroxypropyl benzoate were dissolved in 2 ml of dichloromethane and 0.19 ml (1.05 mmol) of isopropoxytrimethylsilane and 2 μl (0.014 mmol) of trimethylsilyl trifluoromethanesulfonate were sequentially added thereto with stirring under ice-cooling, followed by stirring at the same temperature for 1 hour. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate 1:1), to give 121 mg of ethyl (2R)-2-benzoyloxymethyl-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate as a pale yellow oil (yield: 81%).
Subsequently, 121 mg (0.22 mmol) of this compound was dissolved in 2 ml of a mixture of methanol-tetrahydrofuran (1:1), and to the solution was added 0.5 ml (0.50 mmol) of 1N aqueous sodium hydroxide with stirring under ice-cooling, followed by stirring at the same temperature for 30 minutes. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:1) to give 41 mg of the title compound as an amorphous substance (yield: 41%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.64 (1H, dd, J=9 Hz, 5 Hz), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.06-6.97 (2H, m), 6.89 (0.25H, s), 6.86 (0.25H, s), 6.80 (0.25H, s), 6.78 (0.25H, s), 4.43-4.31 (1.75H, m), 4.26-4.02 (3.25H, m), 3.95-3.87 (0.75H, m), 3.85-3.77 (1H, m), 3.75-3.69 (0.25H, m), 3.68-3.59 (1H, m), 2.65-2.38 (2H, m), 2.25-2.11 (1H, m), 2.11-2.05 (0.25H, m), 2.03-1.97 (0.25H, m), 1.94-1.81 (1.5H, m), 1.26 (3H, t, J=7 Hz).
##STR00028##
6.1 g (16.2 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3-oxo-1-cyclohexene-1-carboxylate obtained in Example 7 was dissolved in 120 ml of methanol and 4.1 g (16.2 mmol) of pyridinium p-toluenesulfonate and 8.86 ml (81.0 mmol) of trimethoxymethane were sequentially added thereto with stirring under ice-cooling, followed by stirring overnight at room temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 6.0 g of the title compound as a white powder (yield: 88%).
Melting point: 97-98° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.07-6.97 (3H, m), 4.41 (1H, d, J=4 Hz), 4.28-4.12 (2H, m), 3.29 (3H, s), 3.23 (3H, s), 2.47-2.38 (1H, m), 2.31-2.21 (1H, m), 2.18-2.06 (1H, m), 2.01-1.93 (1H, m), 1.28 (3H, t, J=7 Hz).
342 mg (0.81 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexen-1-carboxylate obtained in (16a) and 206 mg (1.05 mmol) of (S)-2,3-dihydroxypropyl benzoate were dissolved in 7 ml of dichloromethane, and 0.56 ml (3.15 mmol) of isopropoxytrimethylsilane and 7 μl (0.041 mmol) of trimethylsilyl trifluoromethanesulfonate were added thereto sequentially with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:1), to give 410 mg of ethyl (2S)-2-benzoyloxymethyl-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate as a colorless oil (yield: 91%).
Subsequently, 410 mg (0.74 mmol) of this compound was dissolved in 10 ml of a mixture of methanol-tetrahydrofuran (1:1) and 3 ml (3.0 mmol) of 1N aqueous sodium hydroxide was added thereto, followed by stirring for 15 minutes at room temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:1) to give 293 mg of the title compound as an amorphous substance (yield: 88%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.64 (1H, dd, J=9 Hz, 5 Hz), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.95 (2H, m), 6.89 (0.42H, s), 6.86 (0.02H, s), 6.80 (0.02H, s), 6.78 (0.42H, s), 4.43-4.31 (1.5H, m), 4.26-4.02 (2.5H, m), 3.96-3.89 (1H, m), 3.83-3.77 (0.5H, m), 3.75-3.69 (0.5H, m), 3.68-3.59 (1H, m), 2.65-2.41 (2H, m), 2.25-2.10 (1H, m), 1.93-1.82 (1H, m), 1.77-1.67 (0.5H, br. s), 1.58 (0.5H, br. s), 1.26 (3H, t, J=7 Hz).
##STR00029##
Following the process described in Example (16b), 1,4-di-O-benzoyl-D-threitol was used in place of (S)-2,3-dihydroxypropyl benzoate to give the title compound as an amorphous substance (yield: 44%).
<Alternative Procedure>
1.46 g (3.08 mmol) of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol obtained in Reference Example 18 was suspended in 2 ml of acetonitrile, and 0.04 ml (0.24 mmol) of trimethylsilyl trifluoromethanesulfonate and a solution of 1.00 g (2.37 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) in 5 ml of acetonitrile were sequentially added thereto with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature. The reaction solution was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 1.50 g of the title compound as a pale yellow powder (yield: 92%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 8.10-8.04 (4H, m), 7.68-7.57 (3H, m), 7.49-7.44 (4H, m), 7.16 (1H, dt, J=8.0 Hz, 2.6 Hz), 7.05-7.00 (2H, m), 6.87 (1H, d, J=14.0 Hz), 4.66-4.07 (9H, m), 2.63-2.44 (2H, m), 2.25-2.19 (1H, m), 1.94 (1H, t, J=15.2 Hz), 1.19 (3H, t, J=7.0 Hz).
1.50 g (2.18 mmol) of ethyl (2R,3R)-2,3-bis(benzoyloxymethyl)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in (17a) was dissolved in 10 ml of a mixture of methanol-tetrahydrofuran (4:1), and 10 ml (10.0 mmol) of 1N aqueous sodium hydroxide was added thereto with stirring under ice-cooling, followed by stirring for 15 minutes at the same temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:1) to give 900 mg of the title compound as a white amorphous substance (yield: 86%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.69-7.64 (1H, m), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.99 (2H, m), 6.91-6.90 (0.5H, m), 6.85-6.84 (0.5H, m), 4.43-4.41 (1H, m), 4.27-4.09 (3.5H, m), 4.05-4.01 (0.5H, m), 3.93-3.81 (2H, m), 3.75-3.69 (2H, m), 2.59-2.45 (2H, m), 2.23-1.50 (4H, m), 1.29-1.24 (3H, m).
##STR00030##
Following the process described in Example (16b), 1,4-di-O-benzoyl-L-threitol was used in place of (S)-2,3-dihydroxypropyl benzoate to give the title compound as an amorphous substance (34% yield).
<Alternative Procedure>
Following the process described in Example 17 (alternative procedure), 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-L-threitol obtained in Reference Example 19 was used in place of 1,4-di-o-benzoyl-2,3-di-o-trimethylsilyl-D-threitol to give the title compound as an amorphous substance (yield: 73%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.69-7.64 (1H, m), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.99 (2H, m), 6.91-6.90 (0.5H, m), 6.85-6.84 (0.5H, m), 4.43-4.41 (1H, m) 4.27-4.09 (3.5H, m), 4.05-4.01 (0.5H, m), 3.93-3.81 (2H, m), 3.75-3.69 (2H, m), 2.59-2.45 (2H, m), 2.23-1.50 (4H, m), 1.29-1.24 (3H, m).
##STR00031##
200 mg (0.47 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 290 mg (0.61 mmol) of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-meso-erythritol obtained in Reference Example 1 were dissolved in 4 ml of dichloromethane and 4 μl (0.024 mmol) of trimethylsilyl trifluoromethanesulfonate was added thereto with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 171 mg of ethyl meso-2,3-bis[(benzoyloxy)methyl]-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate as an amorphous substance (yield: 53%).
Subsequently, 170 mg (0.25 mmol) of this compound was dissolved in 10 ml of a mixture of methanol-tetrahydrofuran (1:1), and 3 ml (3.0 mmol) of 1N aqueous sodium hydroxide was added thereto with stirring under ice-cooling, followed by stirring for 15 minutes at the same temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:3) to give 105 mg of the title compound as an amorphous substance (yield: 89%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.64 (1H, dd, J=9 Hz, 5 Hz), 7.15 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.95 (2H, m), 6.93 (0.4H, s), 6.72 (0.6H, s), 4.49-4.33 (2.4H, m), 4.32-4.26 (0.6H, m), 4.25-4.07 (2H, m), 3.93-3.70 (4H, m), 2.69-2.58 (0.4H, m), 2.58-2.35 (3.6H, m), 2.24-2.09 (1H, m), 1.99-1.91 (0.6H, m), 1.90-1.83 (0.4H, m), 1.27 (3H, t, J=7 Hz).
##STR00032##
300 mg (0.71 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 436 mg (1.42 mmol) of (4R,5R)-2,2-dimethyl-4,5-bis[(trimethylsilyl)oxy]methyl[1.3]dioxolane were dissolved in 12 ml of dichloromethane and 26 μl (0.142 mmol) of trimethylsilyl trifluoromethanesulfonate was added thereto with stirring under ice-cooling, followed by stirring for 90 hours at room temperature. Saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with dichloromethane. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=4:1) to give 90 mg of ethyl (2R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2-((4R)-2,2-dimethyl[1.3]dioxolan-4-yl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate as an amorphous substance (yield: 24%).
Subsequently, to 85 mg (0.163 mmol) of this compound was added 4 ml of a mixture of acetic acid-water (1:1), followed by stirring overnight at room temperature. The reaction solution was neutralized with addition of saturated aqueous sodium hydrogencarbonate, and the mixture was then extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 46 mg of the title compound as an amorphous substance (yield: 59%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.69-7.64 (1H, m), 7.19-7.15 (1H, m), 7.06-6.98 (2H, m), 6.89-6.80 (1H, m), 4.43-4.41 (1H, m), 4.38-4.08 (4H, m), 4.03-3.95 (0.7H, m), 3.86 (0.3H, t, J=8 Hz), 3.77-3.63 (3H, m), 2.67-2.37 (3H, m), 2.22-1.84 (3H, m), 1.30-1.25 (3H, m).
##STR00033##
547 mg (1.07 mmol) of 1,3,4,5,7-penta-O-trimethylsilyl-D-arabitol obtained in Reference Example 2 was dissolved in 3 ml of nitromethane, to the resulting solution was added 13 μl (0.007 mmol) of trimethylsilyl trifluoromethanesulfonate and was then added 300 mg (0.71 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature. A saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with dichloromethane. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 151 mg of the title compound as an amorphous substance (yield: 42%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.66 (1H, dd, J=9 Hz, 5 Hz), 7.19-7.15 (1H, m), 7.10-6.99 (2H, m), 6.86 (0.5H, s), 6.82-6.80 (0.5H, m), 4.42-4.39 (1H, m), 4.28-3.65 (9H, m), 3.20-1.40 (3H, br), 2.57-2.43 (2H, m), 2.23-2.09 (1H, m), 1.92-1.82 (1H, m), 1.29-1.25 (3H, m).
##STR00034##
200 mg (0.47 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 434 mg (0.71 mmol) of 1,2,3,4,5,6-hexa-O-trimethylsilyl-D-mannitol were dissolved in 4 ml of dichloromethane, to the resulting solution were added sequentially 0.12 ml (0.47 mmol) of isopropoxytrimethylsilane and 4 μl (0.024 mmol) of trimethylsilyl trifluoromethanesulfonate with stirring under ice-cooling, followed by stirring overnight at room temperature. Saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; dichloromethane:methanol=10:1) to give 130 mg of the title compound as an amorphous substance (yield: 51%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.62 (1H, dd, J=9 Hz, 5 Hz), 7.22-7.12 (2H, m), 7.04-6.96 (1H, m), 6.88-6.84 (0.2H, m), 6.80-6.77 (0.4H, m), 6.76 (0.4H, s), 4.41-4.31 (1H, m), 4.25-4.03 (4H, m), 3.98-3.63 (6H, m), 2.54-2.41 (2H, m), 2.22-2.08 (1H, m), 1.92-1.81 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00035##
Following the process described in Example 19, 1,6-di-O-benzoyl-2,3,4,5-tetra-O-trimethylsilyl-D-mannitol obtained in Reference Example 3 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-meso-erythritol to give the title compound as a white powder (yield: 11%).
Melting point: 55-56° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.20-7.13 (2H, m), 7.06-7.00 (1H, m), 6.80 (0.5H, s), 6.78 (0.5H, s), 4.38 (1H, d, J=5 Hz), 4.26-4.00 (5H, m), 3.98-3.88 (1.5H, m), 3.87-3.65 (5.5H, m), 2.78-2.56 (2H, m), 2.55-2.40 (2H, m), 2.23-2.09 (1H, m), 1.92-1.80 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00036##
Following the process described in Example 19, 2-trimethylsilyloxy-1-trimethylsilyloxymethylethyl adamantan-1-carboxylate obtained in Reference Example 4 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-meso-erythritol to give the title compound as an amorphous substance (yield: 17%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.69-7.64 (1H, m), 7.52-7.51 (0.5H, m), 7.18-7.15 (1H, m), 7.08-6.99 (2.5H, m), 4.45-4.42 (1H, m), 4.31-4.05 (4H, m), 3.88-3.74 (2H, m), 3.72-3.63 (1H, m), 2.78-2.52 (1H, br), 2.48-1.97 (4H, m), 1.31-1.26 (3H, m).
##STR00037##
100 mg (0.266 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3-oxo-1-cyclohexene-1-carboxylate obtained in Example 7 and 156 mg (0.532 mmol) of 5,5-bis[(trimethylsilyl)oxy]methyl[1.3]dioxane were dissolved in 2 ml of dichloromethane and 10 μl (0.053 mmol) of trimethylsilyl trifluoromethanesulfonate was added thereto at −78° C., followed by stirring for 30 minutes at the same temperature and then for 2 hours at room temperature. Saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with dichloromethane. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) and the resulting solid was further washed with isopropyl ether to give 49 mg of the title compound as a white powder (yield: 52%).
Melting point: 156-157° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.66 (1H, dd, J=9 Hz, 5 Hz), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.98 (2H, m), 4.83 (1H, d, J=6 Hz), 4.78 (1H, d, J=6 Hz), 4.44-4.42 (1H, m), 4.29-4.14 (2H, m), 3.87-3.70 (8H, m), 2.44-2.38 (1H, m), 2.32-2.24 (1H, m), 2.18-2.08 (2H, m), 1.28 (3H, t, J=7 Hz).
##STR00038##
500 mg (1.19 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 205 mg (1.54 mmol) of N-(2-hydroxy-1-hydroxymethylethyl)acetamide were dissolved in 20 ml of dichloromethane, and 0.84 ml (4.74 mmol) of isopropoxytrimethylsilane and 43 μl (0.24 mmol) of trimethylsilyl trifluoromethanesulfonate were added sequentially with stirring under ice-cooling, followed by stirring for 30 minutes at the same temperature, and further for 66 hours at room temperature. Saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with dichloromethane. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate methanol=39:1) to give 288 mg of the title compound as an amorphous substance (yield: 50%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.66 (1H, dd, J=9 Hz, 5 Hz), 7.62-7.60 (0.5H, m), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.99 (2H, m), 6.93-6.91 (0.5H, m), 6.35 (1H, br.d, J=8 Hz), 4.46-4.42 (1H, m), 4.35-4.11 (4H, m), 4.03-3.95 (1H, m), 3.82-3.70 (2H, m), 2.60-2.55 (0.5H, m), 2.48-2.01 (3H, m), 2.06 (3H, s), 1.95-1.90 (0.5H, m), 1.30 (3H, t, J=7 Hz).
##STR00039##
500 mg (1.19 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 1.0 g (2.38 mmol) of 1,3-bis[(trimethylsilyl)oxy]-2,2-bis[(trimethylsilyl)oxy]methylpropane were dissolved in 10 ml dichloromethane and 10 μl (0.06 mmol) of trimethylsilyl trifluoromethanesulfonate was added thereto with stirring under ice-cooling, followed by stirring for 2 hours at the same temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 510 mg of the title compound as an amorphous substance (yield: 87%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.66 (1H, dd, J=9 Hz, 5 Hz), 7.28 (1H, s), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.11 (1H, s), 7.07-6.98 (1H, m), 4.42 (1H, d, J=4 Hz), 4.30-4.10 (2H, m), 3.92-3.68 (8H, m), 2.54-2.36 (3H, m), 2.34-2.23 (1H, m), 2.21-2.07 (2H, m), 1.28 (3H, t, J=7 Hz).
##STR00040##
Following the process described in Example 27, diethyl 2,2-bis[(trimethylsilyl)oxy]methylmalonate obtained in Reference Example 5 was used in place of 1,3-bis[(trimethylsilyl)oxy]-2,2-bis[(trimethylsilyl)oxy]methylpropane to give the title compound as an amorphous substance (yield: 42%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.65 (1H, dd, J=9 Hz, 5 Hz), 7.23-7.21 (1H, m), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.99 (1H, m), 6.97 (1H, s), 4.43-4.36 (3H, m), 4.31-4.13 (8H, m), 2.44-2.37 (1H, m), 2.33-2.25 (1H, m), 2.19-2.06 (2H, m), 1.283 (3H, t, J=7 Hz), 1.280 (6H, t, J=7 Hz).
##STR00041##
24.5 ml (24.5 mmol) of 1.0 M diethyl zinc/hexane solution was added to 30 ml of dichloromethane, and then a solution of 1.89 ml (24.5 mmol) of trifluoroacetic acid in 10 ml of dichloromethane was added with stirring under ice-cooling. The reaction solution was stirred for 20 minutes at the same temperature, then a solution of 1.97 ml (24.5 mmol) of diiodomethane in 10 ml of dichloromethane was added and stirred for 20 minutes, and 1.40 g (6.13 mmol) of a solution of diethyl 4-methyleneheptanedicarboxylate (compound described in J.A.C.S. 107, 13, 3981-3997 (1985)) in 10 ml of dichloromethane was further added. After the reaction solution was stirred for 6 hours at room temperature, ice water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=5:1) to give 1.48 g of the title compound as a brown oil (yield: 99%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.10 (2H, q, J=7 Hz), 3.37-2.31 (4H, m), 1.60-1.53 (4H, m), 1.25 (6H, t, J=7 Hz), 0.31 (4H, s).
1.46 g (6.03 mmol) of ethyl 3-[1-(2-ethoxycarbonylethyl)cyclopropyl]propionate obtained in (29a) was dissolved in 60 ml of tetrahydrofuran and 1.35 g (12.1 mmol) of potassium t-butoxide was added thereto, followed by stirring for 1 hour at room temperature. The reaction solution was cooled with ice and made acidic by addition of 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 1.05 g of the title compound as a yellow oil (yield: 89%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 12.23 (0.7H, s), 4.26-4.09 (2H, m), 3.50 (0.3H, dd, J=10 Hz, 6 Hz), 2.57-2.42 (0.7H, m), 2.36 (2H, t, J=6 Hz), 2.03-1.94 (0.3H, m), 1.66-1.52 (1H, m), 1.48 (2H, t, J=6 Hz), 1.28 (3H, J=7 Hz), 0.60-0.30 (4H, m).
1.05 g (5.35 mmol) of ethyl 6-hydroxyspiro[2.5]oct-5-ene-5-carboxylate obtained in (29b) was dissolved in 30 ml of dichloromethane, and 0.99 ml (5.89 mmol) of diisopropylethylamine and 1.40 ml (8.03 mmol) of trifluoromethanesulfonic anhydride were added sequentially with stirring at −78° C. After the reaction solution was stirred for 3 hours at the same temperature, it was warmed to room temperature. The reaction solution was poured into saturated aqueous sodium hydrogencarbonate and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 1.56 g of the title compound as a brown oil (yield: 89%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.26 (2H, q, J=7 Hz), 2.57-2.46 (2H, m), 2.35-2.29 (2H, m), 1.60-1.53 (2H, m), 1.32 (3H, t, J=7 Hz), 0.49-0.40 (4H, m).
Following the process described in Example (1a), ethyl 6-trifluoromethanesulfonyloxyspiro[2.5]oct-5-ene-5-carboxylate obtained in (29c) was used in place of ethyl 8-trifluoromethanesulfonyloxy-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to give ethyl 6-acetylsulfanylspiro[2.5]oct-5-ene-5-carboxylate as a pale yellow oil (yield: 58%).
Subsequently, 700 mg (2.75 mmol) of this compound was dissolved in 14 ml of ethanol, and 2.75 ml (11 mmol) of 4N hydrogen chloride/dioxane solution was added thereto with stirring under ice-cooling, followed by stirring for 4 hours at room temperature. The reaction solution was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=10:1), to give 300 mg of the title compound as a pale yellow oil (yield: 51%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.19 (2H, q, J=7 Hz), 4.12 (1H, s), 2.57 (2H, t, J=6 Hz), 2.22-2.18 (2H, m), 1.46 (2H, t, J=6 Hz), 1.29 (3H, t, J=7 Hz), 0.40-0.33 (4H, m).
7 ml of acetic acid was added to 651 mg (4.23 mmol) of sodium perborate tetrahydrate, the mixture was heated to 50° C., and a solution of 300 mg (1.41 mmol) of ethyl 6-mercaptospiro[2.5]oct-5-ene-5-carboxylate obtained in (29d) in 3 ml of acetic acid was added thereto, followed by stirring for 2 hours at the same temperature and further for 3 hours at 80° C. The reaction solution was cooled to room temperature and concentrated under reduced pressure. 5 ml of thionyl chloride was added to the residue, and the mixture was heated under reflux for 2 hours. The reaction solution was cooled to room temperature again and concentrated under reduced pressure. Ice water was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=5:1 to give 195 mg of the title compound as a colorless oil (yield: 50%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 4.28 (2H, q, J=7 Hz), 2.77-2.69 (2H, m), 2.43-2.38 (2H, m), 1.62 (2H, t, J=6 Hz), 1.33 (3H, t, J=7 Hz), 0.52-0.46 (4H, m).
Following the process described in Example (1d), ethyl 6-(chlorosulfonyl)spiro[2.5]oct-5-ene-5-carboxylate obtained in (29e) was used in place of ethyl 8-chlorosulfonyl-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to give the title compound as a white powder (yield: 17%).
Melting point: 125-126° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm: 7.69 (1H, dd, J=9 Hz, 5 Hz), 7.13 (1H, dd, J=8 Hz, 3 Hz), 7.03-6.96 (2H, m), 6.58 (1H, s), 4.53 (1H, d, J=5 Hz), 4.20-4.04 (2H, m), 2.62-2.50 (2H, m), 1.98-1.85 (1H, m), 1.23 (3H, t, J=7 Hz), 1.22-1.13 (1H, m), 1.09-0.99 (2H, m), 0.93-0.80 (2H, m).
##STR00042##
430 mg (5 mmol) of γ-butyrolactone was dissolved in 10 ml of tetrahydrofuran, and 22 ml (11 mmol) of 0.5 M (1,3-dioxan-2-ylethyl)magnesium bromide/tetrahydrofuran solution was added thereto with stirring under ice-cooling, followed by stirring for 3 hours at 50° C. After the reaction solution was cooled with ice, saturated aqueous ammonium chloride was added and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate:ethanol=10:1) to give 880 mg of the title compound as a colorless oil (yield: 55%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.51 (2H, t, J=5 Hz), 4.08 (4H, dd, J=10 Hz, 4 Hz), 3.79-3.70 (4H, m), 3.61 (2H, t, J=6 Hz), 2.13-2.00 (2H, m), 1.68-1.56 (12H, m), 1.55-1.49 (2H, m), 1.37-1.29 (2H, m).
2.60 g (8.17 mmol) of 7-(1,3-dioxan-2-yl)-5-[2-(1,3-dioxan-2-yl)ethyl]heptane-1,5-diol obtained in (30a) was dissolved in 45 ml of pyridine, and a solution of 1.64 g (8.58 mmol) of p-toluenesulfonyl chloride in 15 ml of pyridine was added thereto with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature and further for 3 hours at room temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:1) to give 1.31 g of the title compound as a colorless oil (yield: 53%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.50 (2H, t, J=5 Hz), 4.09 (2H, dd, J=11 Hz, 5 Hz), 3.83-3.68 (6H, m), 2.15-1.99 (2H, m), 1.92-1.82 (2H, m), 1.73-1.48 (12H, m), 1.38-1.29 (2H, m).
1.31 g (43.6 mmol) of 2-(2-{(2-[2-(1,3-dioxan-2-yl)ethyl]tetrahydrofuran-2-yl}ethyl)-1,3-dioxane obtained in (30b) was dissolved in 15 ml of acetone, and 16.3 ml (43.6 mmol) of Jones reagent was added thereto with stirring under ice-cooling, followed by stirring for 3 hours at room temperature. The reaction solution was cooled with ice, and then the reaction was terminated by addition of isopropyl alcohol. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was dissolved in 15 ml of ethanol, and 0.76 ml (10.5 mmol) of thionyl chloride was added, followed by stirring overnight at room temperature. The reaction solution was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=1:1) to give 610 mg of the title compound as a yellow oil (yield: 51%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.13 (4H, q, J=7 Hz), 3.78 (2H, t, J=7 Hz), 2.37-2.31 (4H, m), 1.95-1.87 (2H, m), 1.86-1.79 (4H, m) 1.71 (2H, t, J=7 Hz), 1.26 (6H, t, J=7 Hz).
610 mg (2.24 mmol) of ethyl 3-[2-(2-ethoxycarbonylethyl)tetrahydrofuran-2-yl]propionate obtained in (30c) was dissolved in 18 ml of tetrahydrofuran, and 503 mg (4.48 mmol) of potassium t-butoxide was added thereto, followed by heating under reflux for 1 hour. After the reaction solution was cooled with ice, the reaction solution was made acidic by addition of 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 340 mg of the title compound as a colorless oil (yield: 67%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
12.24 (1H, s), 4.26-4.12 (2H, m), 3.96-3.79 (2H, m), 2.63-2.47 (1H, m), 2.43-2.12 (3H, m), 2.05-1.86 (2H, m), 1.86-1.60 (4H, m), 1.30 (3H, t, J=7 Hz).
To a suspension of 72 mg of 55% sodium hydride (1.65 mmol)/3 ml of dichloromethane, was added a solution of 340 mg (1.50 mmol) of ethyl 8-oxo-1-oxaspiro[4.5]decane-7-carboxylate obtained in (29d) in 4 ml of dichloromethane with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature. Subsequently, the reaction solution was cooled to −78° C., and 0.28 ml (1.65 mmol) of trifluoromethanesulfonic anhydride was added thereto. The mixture was stirred for 1 hour at the same temperature, and then warmed to room temperature. After ice water was added to the reaction solution to terminate the reaction, the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 480 mg of the title compound as a pale yellow oil (yield: 89%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.26 (2H, q, J=7 Hz), 3.92-3.81 (2H, m), 2.74-2.63 (1H, m), 2.62-2.48 (2H, m), 2.45-2.34 (1H, m), 2.04-1.68 (6H, m), 1.32 (3H, t, J=7 Hz).
Following the process described in Example (1a), ethyl 8-trifluoromethanesulfonyloxy-1-oxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (30e) was used in place of ethyl 8-trifluoromethanesulfonyloxy-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to give the title compound as a yellow oil (yield: 32%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.18 (2H, q, J=7 Hz), 3.91-3.83 (2H, m), 2.65-2.60 (1H, m), 2.60-2.51 (2H, m), 2.40-2.35 (1H, m), 2.32 (2.6H, s), 2.29 (0.4H, s), 2.00-1.93 (2H, m), 1.87-1.67 (4H, m), 1.28 (3H, t, J=7 Hz).
120 mg (0.42 mmol) of ethyl 8-acetylthio-1-oxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (30f) was dissolved in 3 ml of ethanol, and 1 ml (4 mmol) of 4N hydrogen chloride/dioxane solution was added thereto, followed by stirring for 4 hours at room temperature. The reaction solution was concentrated under reduced pressure and the residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1) to give 100 mg of the title compound as a pale yellow oil (98% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.24-4.16 (2H, m), 4.12 (1H, s), 3.91-3.80 (2H, m), 2.84-2.71 (1H, m), 2.52-2.34 (3H, m), 2.01-1.90 (2H, m), 1.82-1.58 (4H, m), 1.23 (3H, t, J=7 Hz).
100 mg (0.41 mmol) of ethyl 8-mercapto-1-oxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (30f) was dissolved in 4 ml of solution mixture of acetic acid and water (acetic acid:water=1:1), and chlorine gas was blown into the reaction solution with stirring under ice-cooling for 15 minutes. Ice water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1) to give 108 mg of the title compound as a colorless oil (yield: 85%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.28 (2H, q, J=7 Hz), 3.88 (2H, t, J=7 Hz), 2.92-2.81 (1H, m), 2.77-2.66 (1H, m), 1.58 (2H, m), 2.06-1.89 (3H, m), 1.80 (2H, t, 7 Hz), 1.77-1.67 (1H, m), 1.34 (3H, t, J=7 Hz).
To a solution of 57 mg (0.39 mmol) of 2-chloro-4-fluoroaniline and 0.05 ml (0.39 mmol) of triethylamine in 1 ml of ethyl acetate, was added dropwise a solution of 108 mg (0.35 mmol) of ethyl 8-chlorosulfonyl-1-oxaspiro[4.5]dec-7-ene-7-carboxylate obtained in (29h) in 2 ml of ethyl acetate with stirring under ice-cooling, followed by stirring overnight at room temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel thin layer chromatography (solvent; hexane:ethyl acetate=3:1) to give 12 mg of low polarity diastereomer of the title compound as a white powder and 20 mg of high polarity diastereomer of the title compound as an amorphous substance (yield: 8%, 14%).
(Low Polarity Diastereomer)
Melting point: 112-114° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.65 (1H, dd, J=9 Hz, 5 Hz), 7.14 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.97 (1H, m), 6.95 (1H, s), 6.90 (1H, s), 4.45 (1H, dd, J=6 Hz, 2 Hz), 4.22-4.10 (2H, m), 3.96-3.88 (1H, m), 3.86-3.79 (1H, m), 2.41-2.33 (1H, m), 2.29-2.18 (1H, m), 2.13-2.01 (4H, m), 1.94-1.79 (2H, m), 1.25 (3H, t, J=7 Hz).
(High Polarity Diastereomer)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=9 Hz, 5 Hz), 7.13 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.96 (2H, m), 6.95 (1H, s), 4.36 (1H, d, J=5 Hz), 4.22-4.10 (2H, m), 4.03-3.96 (1H, m), 3.93-3.85 (1H, m), 2.56-2.48 (1H, m), 2.40-2.29 (1H, m), 2.06-1.63 (6H, m), 1.26 (3H, t, J=7 Hz).
##STR00043##
To a solution of 1.0 g (12.18 mmol) of 1H-pyrrol-1-ylamine and 1.8 ml (13.40 mmol) of triethylamine in 60 ml of ethyl acetate was added dropwise a solution of 3.6 g (12.18 mmol) of ethyl 2-chlorosulfonyl-1-cyclohexene-1-carboxylate (compound disclosed in the specification of Japanese Patent Application (Kokai) No. 2000-178246) in 12 ml of ethyl acetate with stirring under ice-cooling, followed by stirring overnight at room temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1) and the resulting solid was further washed with isopropyl ether to give 1.9 g of the title compound as a white powder (yield: 52%).
Melting point: 85-86° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.15 (1H, s), 7.44-7.42 (1H, m), 7.02 (2H, t, J=2 Hz), 6.17 (2H, t, J=2 Hz), 4.57-4.56 (1H, m), 4.29 (2H, q, J=7 Hz), 2.52-2.46 (2H, m), 2.32-2.23 (1H, m), 1.93-1.66 (3H, m), 1.34 (3H, t, J=7 Hz).
##STR00044##
Following the process described in Example 31, 2-methyl-1H-pyrrol-1-ylamine was used in place of 1H-pyrrol-1-ylamine to give the title compound as a white powder (yield: 32%).
Melting point: 100-101° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.95 (1H, s), 7.43-7.39 (1H, m), 7.03-6.99 (1H, m), 6.07 (1H, t, J=4 Hz), 5.88-5.84 (1H, m), 4.60-4.55 (1H, m), 4.26 (2H, q, J=7 Hz), 2.56-2.43 (2H, m), 2.34-2.20 (1H, m), 2.29 (3H, s), 1.95-1.66 (3H, m), 1.33 (3H, t, J=7 Hz).
##STR00045##
Following the process described in Example 31, 2-ethyl-1H-pyrrol-1-ylamine was used in place of 1H-pyrrol-1-ylamine to give the title compound as a white powder (yield: 51%).
Melting point: 77-78° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.97 (1H, s), 7.46-7.41 (1H, m), 7.04-7.01 (1H, m), 6.13 (1H, t, J=4 Hz), 5.92-5.87 (1H, m), 4.62-4.57 (1H, m), 4.28 (2H, q, J=7 Hz), 2.79-2.64 (2H, m), 2.58-2.42 (2H, m), 2.35-2.21 (1H, m), 1.95-1.65 (3H, m), 1.33 (3H, t, J=7 Hz), 1.24 (3H, t, J=8 Hz).
##STR00046##
Following the process described in Example 31, 2-propyl-1H-pyrrol-1-ylamine was used in place of 1H-pyrrol-1-ylamine to give the title compound as a white powder (yield: 31%).
Melting point: 66-68° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.97 (1H, s), 7.46-7.41 (1H, m), 7.04-7.01 (1H, m), 6.12 (1H, t, J=3 Hz), 5.92-5.87 (1H, m), 4.62-4.57 (1H, m), 4.27 (2H, q, J=7 Hz), 2.73-2.62 (2H, m), 2.57-2.43 (2H, m), 2.34-2.21 (1H, m) 1.95-1.63 (5H, m), 1.33 (3H, t, J=7 Hz), 0.99 (3H, t, J=7 Hz).
##STR00047##
Following the process described in Example 31, 2-butyl-1H-pyrrol-1-ylamine was used in place of 1H-pyrrol-1-ylamine to give the title compound as a white powder (yield: 26%).
Melting point: 49-50° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.94 (1H, s), 7.43-7.39 (1H, m), 7.01-6.98 (1H, m), 6.11-6.08 (1H, m), 5.89-5.85 (1H, m), 4.60-4.55 (1H, m), 4.26 (2H, q, J=7 Hz), 2.71-2.65 (2H, m), 2.56-2.43 (2H, m), 2.33-2.20 (1H, m) 1.94-1.57 (5H, m), 1.45-1.35 (2H, m), 1.32 (3H, t, J=7 Hz), 0.93 (3H, t, J=7 Hz).
##STR00048##
Following the process described in Example 31, 2-pentyl-1H-pyrrol-1-ylamine obtained in Reference Example 6 was used in place of 1H-pyrrol-1-ylamine to give the title compound as a white powder (yield: 33%).
Melting point: 60-61° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.96 (1H, s), 7.46-7.41 (1H, m), 7.04-7.00 (1H, m), 6.12 (1H, t, J=3 Hz), 5.92-5.86 (1H, m), 4.62-4.56 (1H, m), 4.28 (2H, q, J=7 Hz), 2.72-2.65 (2H, m), 2.57-2.44 (2H, m), 2.34-2.21 (1H, m), 1.95-1.59 (5H, m), 1.42-1.29 (4H, m), 1.34 (3H, t, J=7 Hz), 0.89 (3H, t, J=7 Hz).
##STR00049##
Following the process described in Example 31, 2-hexyl-1H-pyrrol-1-ylamine obtained in Reference Example 7 was used in place of 1H-pyrrol-1-ylamine to give the title compound as a yellow oil (yield: 46%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.93 (1H, s), 7.43-7.39 (1H, m), 7.01-6.98 (1H, m), 6.12-6.08 (1H, m), 5.89-5.85 (1H, m), 4.60-4.55 (1H, m), 4.27 (2H, q, J=′ Hz), 2.71-2.64 (2H, m), 2.56-2.43 (2H, m), 2.33-2.21 (1H, m), 1.91-1.58 (5H, m), 1.42-1.27 (6H, m), 1.33 (3H, t, J=7 Hz), 0.88 (3H, t, J=7 Hz).
##STR00050##
Following the process described in Example 31, 2-heptyl-1H-pyrrol-1-ylamine obtained in Reference Example 8 was used in place of 1H-pyrrol-1-ylamine to give the title compound as a colorless oil (yield: 13%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.97 (1H, s), 7.46-7.41 (1H, m), 7.04-7.01 (1H, m), 6.11 (1H, t, J=3 Hz), 5.96-5.86 (1H, m), 4.62-4.56 (1H, m), 4.28 (2H, q, J=7 Hz), 2.72-2.62 (2H, m), 2.58-2.43 (2H, m), 2.35-2.21 (1H, m), 1.94-1.59 (5H, m), 1.41-1.22 (8H, m), 1.33 (3H, t, J=7 Hz), 0.88 (3H, t, J=7 Hz).
##STR00051##
Following the process described in Example 31, 2-octyl-1H-pyrrol-1-ylamine obtained in Reference Example 8 was used in place of 1H-pyrrol-1-ylamine to give the title compound as a pale yellow oil (yield: 18%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.96 (1H, s), 7.46-7.41 (1H, m), 7.04-7.00 (1H, m), 6.11 (1H, t, J=4 Hz), 5.91-5.86 (1H, m), 4.61-4.57 (1H, m), 4.28 (2H, q, J=7 Hz), 2.71-2.64 (2H, m), 2.57-2.44 (2H, m), 2.34-2.20 (1H, m), 1.95-1.58 (5H, m), 1.42-1.19 (10H, m), 1.33 (3H, t, J=7 Hz), 0.88 (3H, t, J=7 Hz).
##STR00052##
Following the process described in Example 31, 2-cyclopropyl-1H-pyrrol-1-ylamine obtained in Reference Example 10 was used in place of 1H-pyrrol-1-ylamine to give the title compound as a pale pink powder (yield: 42%).
Melting point: 95-96° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.87 (1H, s), 7.41-7.37 (1H, m), 6.98-6.95 (1H, m), 6.05-6.02 (1H, m), 5.69-5.66 (1H, m), 4.66-4.61 (1H, m), 4.25 (2H, q, J=7 Hz), 2.60-2.43 (2H, m), 2.34-2.20 (1H, m), 2.05-1.87 (2H, m), 1.82-1.68 (2H, m), 1.31 (3H, t, J=7 Hz), 0.94-0.82 (2H, m), 0.73-0.65 (1H, m), 0.59-0.51 (1H, m).
##STR00053##
Following the process described in Example 31, 2-phenyl-1H-pyrrol-1-ylamine was used in place of 1H-pyrrol-1-ylamine to give the title compound as a pale yellow powder (yield: 21%).
Melting point: 160-161° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.99 (1H, s), 7.57 (2H, d, J=8 Hz), 7.39 (2H, t, J=8 Hz), 7.33-7.27 (2H, m), 7.14-7.11 (1H, m), 6.32-6.28 (1H, m), 6.25 (1H, t, J=4 Hz), 4.22 (2H, q, J=7 Hz), 4.18-4.14 (1H, m), 2.44-2.32 (1H, m), 2.24-2.07 (2H, m), 1.91-1.75 (1H, m), 1.67-1.51 (1H, m), 1.40-1.29 (1H, m), 1.28 (3H, t, J=7 Hz).
##STR00054##
Following the process described in Example 31, 2,5-dimethyl-1H-pyrrol-1-ylamine was used in place of 1H-pyrrol-1-ylamine to give the title compound as a white powder (yield: 29%).
Melting point: 96-97° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.88 (1H, s), 7.40-7.35 (1H, m), 5.75 (2H, s), 4.58-4.52 (1H, m), 4.24 (2H, q, 7 Hz), 2.69-2.61 (1H, m), 2.53-2.42 (1H, m), 2.33-2.19 (1H, m), 2.26 (6H, s), 2.02-1.91 (1H, m), 1.86-1.73 (2H, m), 1.30 (3H, t, J=7 Hz).
##STR00055##
150 mg (0.503 mmol) of ethyl 6-[N-(1H-pyrrol-1-yl)sulfamoyl]-1-cyclohexene-1-carboxylate obtained in Example 31 was dissolved in 3 ml of tetrahydrofuran, and 70 mg (0.528 mmol) of N-chlorosuccinimide was added thereto with stirring under ice-cooling, followed by stirring overnight at room temperature. Water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel thin layer chromatography (solvent; hexane:ethyl acetate=2:1) and the resulting solid was further washed with isopropyl ether to give 50 mg of the title compound as a white powder (yield: 30%).
Melting point: 60-61° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.91 (1H, s), 7.43-7.37 (1H, m), 7.04 (1H, dd, J=4 Hz, 2 Hz), 6.14 (1H, t, J=4 Hz), 6.10 (1H, dd, J=4 Hz, 2 Hz), 4.65-4.61 (1H, m), 4.26 (2H, q, J=7 Hz), 2.61-2.44 (2H, m), 2.33-2.21 (1H, m), 2.05-1.90 (1H, m), 1.83-1.71 (2H, m), 1.30 (3H, t, J=7 Hz).
##STR00056##
Following the process described in Example 43, N-bromosuccinimide was used in place of N-chlorosuccinimide to give the title compound as a white powder (yield: 50%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.85 (1H, s), 7.42-7.38 (1H, m), 7.15 (1H, dd, J=4 Hz, 2 Hz), 6.22-6.17 (2H, m), 4.67-4.62 (1H, m), 4.25 (2H, q, J=7 Hz), 2.60-2.44 (2H, m), 2.33-2.20 (1H, m), 2.05-1.92 (1H, m), 1.83-1.70 (2H, m), 1.30 (3H, t, J=7 Hz).
##STR00057##
Following the process described in Example 42, 2.1 equivalent of N-chlorosuccinimide was used relative to ethyl 6-[N-(1H-pyrrol-1-yl)sulfamoyl]-1-cyclohexene-1-carboxylate obtained in Example 31 to give the title compound as a pale yellow oil (yield: 25%).
Melting point: 144-145° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.08 (1H, s), 7.39-7.33 (1H, m), 6.07 (2H, s), 4.89-4.83 (1H, m), 4.24 (2H, q, J=7 Hz), 2.67-2.58 (1H, m), 2.52-2.42 (1H, m), 2.31-2.19 (1H, m), 2.03-1.88 (1H, m), 1.87-1.72 (2H, m), 1.29 (3H, t, J=7 Hz).
##STR00058##
Following the process described in Example 44, 2.1 equivalent of N-bromosuccinimide was used relative to ethyl 6-[N-(1H-pyrrol-1-yl)sulfamoyl]-1-cyclohexene-1-carboxylate obtained in Example 31 to give the title compound as a white powder (yield: 3%).
Melting point: 123-124° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.05 (1H, s), 7.40-7.35 (1H, m), 6.24 (2H, s), 5.02-4.95 (1H, m), 4.25 (2H, q, J=7 Hz), 2.69-2.60 (1H, m), 2.53-2.42 (1H, m), 2.33-2.19 (1H, m), 2.02-1.90 (1H, m), 1.87-1.72 (2H, m), 1.29 (3H, t, J=7 Hz).
##STR00059##
1.8 g (4.29 mmol) of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 1 was dissolved in 60 ml of a water-tetrahydrofuran (1:1) solution, and 900 mg (21.45 mmol) of lithium hydroxide was added thereto, followed by stirring for 7 hours at 50° C. The reaction solution was cooled with ice, it was then made acidic by addition of 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was washed with hexane to give 1.43 g of the title compound as a pale brown powder (yield: 85%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.04-6.93 (3H, m), 4.36 (1H, d, J=5 Hz), 4.16-4.02 (3H, m), 3.97-3.88 (1H, m), 2.57-2.45 (3H, m), 2.25-2.13 (1H, m), 1.90-1.82 (1H, m).
100 mg (0.26 mmol) of 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylic acid obtained in (47a) was dissolved in 2 ml of toluene, and 1 ml of N,N-dimethylformamide di-t-butyl acetal was added thereto, followed by stirring for 3 hours at 100° C. After the reaction solution was cooled to room temperature, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel thin layer chromatography (solvent; dichloromethane:methanol=1:50) to give 52 mg of the title compound as a white amorphous substance (yield: 45%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.64 (1H, dd, J=9 Hz, 5 Hz), 7.15 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.98 (2H, m), 6.71 (1H, s), 4.42-4.38 (1H, m), 4.13-4.01 (3H, m), 3.95-3.88 (1H, m), 2.51-2.40 (2H, m), 2.21-2.10 (1H, m), 1.86-1.79 (1H, m), 1.46 (9H, s).
Following the process described in Example (47b), various corresponding acetals were used in place of N,N-dimethylformamide di-t-butyl acetal to synthesize the compounds of Examples 48 to 51.
##STR00060##
White powder (yield: 50%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.06-6.99 (1H, m), 6.98 (1H, s), 6.84 (1H, s), 4.43-4.38 (1H, m), 4.15-3.99 (3H, m), 3.95-3.88 (1H, m), 3.73 (3H, s), 2.56-2.43 (2H, m), 2.24-2.12 (1H, m), 1.88-1.79 (1H, m).
##STR00061##
White amorphous substance (yield: 18%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.97 (2H, m), 6.81 (1H, s), 4.42 (1H, d, J=5 Hz), 4.16-3.99 (5H, m), 3.95-3.88 (1H, m), 2.55-2.44 (2H, m), 2.24-2.11 (1H, m), 1.88-1.81 (1H, m), 1.71-1.60 (2H, m), 0.94 (3H, t, J=7 Hz).
##STR00062##
White powder (yield: 26%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.96 (2H, m), 6.80 (1H, s), 4.42 (1H, d, J=5 Hz), 4.20-4.00 (5H, m), 3.95-3.87 (1H, m), 2.55-2.44 (2H, m), 2.24-2.11 (1H, m), 1.88-1.80 (1H, m), 1.66-1.57 (2H, m), 1.43-1.32 (2H, m), 0.93 (3H, t, J=7 Hz).
##STR00063##
White powder (yield: 21%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.06-6.98 (2H, m), 6.78 (1H, s), 5.11-4.99 (1H, m), 4.42 (1H, d, J=5 Hz), 4.15-3.99 (3H, m), 3.95-3.88 (1H, m), 2.55-2.43 (2H, m), 2.24-2.11 (1H, m), 1.99-1.79 (1H, m), 1.26 (3H, d, J=2 Hz), 1.24 (3H, d, J=2 Hz).
##STR00064##
1 g (2.55 mmol) of 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylic acid obtained in Example 47a was dissolved in 20 ml of acetonitrile, and 0.50 ml (5.10 mmol) of bromomethyl acetate, 499 mg (1.53 mmol) of cesium carbonate and 471 mg (1.28 mmol) of tetrabutylammonium iodide were added thereto, followed by stirring for 1 hour at room temperature. 0.1 N hydrochloric acid was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; dichloromethane:methanol=49:1) to give 833 mg of the title compound as an amorphous substance (yield: 70%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.18 (1H, dd, J=8 Hz, 3 Hz), 7.08-7.02 (1H, m), 7.01 (1H, s), 6.92 (1H, s), 5.80 (2H, s), 4.41 (1H, dd, J=6 Hz, 2 Hz), 4.15-4.01 (3H, m), 3.94-3.88 (1H, m), 2.48 (1H, td, J=14 Hz, 4 Hz), 2.44-2.37 (1H, m), 2.22-2.14 (1H, m), 2.12 (3H, s), 1.85-1.79 (1H, m).
Following the process described in Example (1d), various corresponding anilines were used in place of 2-chloro-4-fluoroaniline to synthesize the compounds of Examples 53 to 121.
##STR00065##
Oil (yield: 61%)
1H-NMR spectrum (400 MHz, CDC3) δ ppm:
7.67-7.62 (1H, m), 7.17-7.09 (3H, m), 6.96 (1H, d, J=3 Hz), 6.83 (1H, t, J=1 Hz), 4.43-4.40 (1H, m), 4.24-4.01 (5H, m), 3.95-3.89 (1H, m), 2.55-2.41 (2H, m), 2.21-2.10 (1H, m), 1.89-1.81 (1H, m), 1.27 (3H, t, J=7 Hz).
##STR00066##
Pale brown powder (yield: 69%)
Melting point: 157-160° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.70 (1H, dd, J=8 Hz, 1 Hz), 7.39 (1H, dd, J=8 Hz, 2 Hz), 7.31-7.26 (1H, m), 7.10-7.05 (2H, m), 6.83 (1H, t, J=1 Hz), 4.49-4.46 (1H, m), 4.24-4.02 (5H, m), 3.95-3.89 (1H, m), 2.60-2.48 (2H, m), 2.24-2.13 (1H, m), 1.88-1.81 (1H, m), 1.24 (3H, t, J=7 Hz).
##STR00067##
Oil (yield: 59%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.70 (1H, dd, J=8 Hz, 1 Hz), 7.55 (1H, dd, J=8 Hz, 2 Hz), 7.36-7.30 (1H, m), 7.04-6.98 (2H, m), 6.83 (1H, t, J=1 Hz), 4.50-4.47 (1H, m), 4.23-4.01 (5H, m), 3.95-3.88 (1H, m), 2.62-2.49 (2H, m), 2.24-2.13 (1H, m), 1.88-1.81 (1H, m), 1.24 (3H, t, J=7 Hz).
##STR00068##
Amorphous substance (yield: 53%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.79 (1H, dd, J=8 Hz, 1 Hz), 7.67 (1H, dd, J=8 Hz, 1 Hz), 7.38-7.33 (1H, m), 6.88-6.82 (3H, m), 4.49 (1H, d, J=5 Hz), 4.24-4.01 (5H, m), 3.95-3.88 (1H, m), 2.63-2.49 (2H, m), 2.24-2.13 (1H, m), 1.88-1.81 (1H, m), 1.24 (3H, t, J=7 Hz).
##STR00069##
White powder (yield: 87%)
Melting point: 141-146° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.38-7.33 (2H, m), 7.07-7.01 (3H, m), 6.87 (1H, t, J=1 Hz), 4.30-4.21 (3H, m), 4.14-4.01 (3H, m), 3.95-3.89 (1H, m), 2.45-2.38 (1H, m), 2.27 (1H, td, J=14 Hz, 3 Hz), 2.09-1.99 (1H, m), 1.87-1.80 (1H, m), 1.33 (3H, t, J=7 Hz).
##STR00070##
White powder (yield: 81%)
Melting point: 153-156° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.31 (4H, s), 7.03 (1H, s), 6.87 (1H, t, J=1 Hz), 4.29-4.19 (3H, m), 4.14-4.02 (3H, m), 3.95-3.89 (1H, m), 2.47-2.40 (1H, m), 2.27 (1H, td, J=14 Hz, 3 Hz), 2.10-2.00 (1H, m), 1.88-1.81 (1H, m), 1.32 (3H, t, J=7 Hz).
##STR00071##
White powder (yield: 75%)
Melting point: 101-104° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.56-7.53 (1H, m), 7.23-7.18 (2H, m), 7.11-7.06 (1H, m), 6.85 (1H, t, J=1 Hz), 6.62 (1H, s), 4.44 (1H, dd, J=6 Hz, 2 Hz), 4.25-4.01 (5H, m), 3.95-3.89 (1H, m), 2.55-2.48 (1H, m), 2.42 (1H, td, J=14 Hz, 4 Hz), 2.34 (3H, s), 2.19-2.09 (1H, m), 1.88-1.81 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00072##
White powder (yield: 66%)
Melting point: 83-87° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.54 (1H, dd, J=8 Hz, 1 Hz), 7.25-7.19 (2H, m), 7.14 (1H, td, J=7 Hz, 1 Hz), 6.85 (1H, s), 6.63 (1H, s), 4.47 (1H, dd, J=6 Hz, 2 Hz), 4.25-4.02 (5H, m), 2.75-2.66 (2H, m), 2.54-2.48 (1H, m), 2.43 (1H, td, J=14 Hz, 4 Hz), 2.19-2.11 (1H, m), 1.87-1.81 (1H, m), 1.28-1.23 (6H, m).
##STR00073##
Oil (53% yield)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.55-7.52 (1H, m), 7.23-7.18 (2H, m), 7.14-7.09 (1H, m), 6.85 (1H, t, J=1 Hz), 6.64 (1H, s), 4.48-4.44 (1H, m), 4.24-4.02 (5H, m), 3.95-3.89 (1H, m), 2.67-2.62 (2H, m), 2.54-2.39 (2H, m), 2.20-2.10 (1H, m), 1.87-1.81 (1H, m), 1.69-1.58 (2H, m), 1.26 (3H, t, J=7 Hz), 0.99 (3H, t, J=7 Hz).
##STR00074##
Oil (yield: 19%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=8 Hz, 1 Hz), 7.47 (1H, dd, J=8 Hz, 2 Hz), 7.37 (1H, td, J=8 Hz, 2 Hz), 7.21 (1H, s), 7.07 (1H, td, J=8 Hz, 1 Hz), 6.82 (1H, t, J=1 Hz), 4.52-4.49 (1H, m), 4.22-4.01 (5H, m), 3.95-3.88 (1H, m), 3.49 (1H, s), 2.65-2.50 (2H, m), 2.24-2.13 (1H, m), 1.88-1.81 (1H, m), 1.22 (3H, t, J=7 Hz).
##STR00075##
Pale brown powder (yield: 65%)
Melting point: 115-118° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.53-7.49 (1H, m), 7.34-7.30 (1H, m), 7.23-7.17 (2H, m), 6.86 (1H, s), 6.69 (1H, s), 4.47 (1H, dd, J=6 Hz, 2 Hz), 4.27-4.02 (5H, m), 3.95-3.89 (1H, m), 3.33-3.24 (1H, m), 2.53-2.47 (1H, m), 2.42 (1H, td, J=14 Hz, 3 Hz), 2.18-2.10 (1H, m), 1.86-1.81 (1H, m), 1.29-1.21 (9H, m).
##STR00076##
White powder (yield: 53%)
Melting point: 117-120° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.45 (1H, dd, J=8 Hz, 1 Hz), 7.38 (1H, dd, J=8 Hz, 2 Hz), 7.23 (1H, td, J=8 Hz, 2 Hz), 7.12-7.07 (1H, m), 6.86 (1H, t, J=1 Hz), 6.64 (1H, s), 4.64-4.61 (1H, m), 4.24-4.03 (5H, m), 3.97-3.90 (1H, m), 2.65-2.53 (2H, m), 2.28-2.18 (1H, m), 1.90-1.83 (1H, m), 1.45 (9H, s), 1.23 (3H, t, J=7 Hz).
##STR00077##
Oil (71% yield)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.54-7.49 (1H, m), 7.29-7.16 (3H, m), 6.86 (1H, dt, J=5 Hz, 1 Hz), 6.68 (1H, d, J=10 Hz), 4.47-4.44 (1H, m), 4.27-4.02 (5H, m) 3.95-3.89 (1H, m), 3.12-2.95 (1H, m), 2.53-2.35 (2H, m), 2.19-2.07 (1H, m), 1.86-1.80 (1H, m), 1.70-1.55 (2H, m), 1.31-1.19 (6H, m), 0.91-0.80 (3H, m).
##STR00078##
White powder (yield: 70%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.57 (1H, dd, J=8 Hz, 2 Hz), 7.11-7.05 (2H, m), 6.96 (1H, td, J=8 Hz, 1 Hz), 6.89 (1H, dd, J=8 Hz, 1 Hz), 6.79 (1H, t, J=1 Hz), 4.44 (1H, d, J=4 Hz), 4.21-4.00 (5H, m), 3.94-3.84 (4H, m), 2.58 (1H, td, J=14 Hz, 4 Hz), 2.50-2.43 (1H, m), 2.18-2.08 (1H, m), 1.84-1.77 (1H, m), 1.23 (3H, t, J=7 Hz).
##STR00079##
White powder (yield: 60%)
Melting point: 129-134° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.58 (1H, dd, J=8 Hz, 2 Hz), 7.12 (1H, s), 7.06 (1H, td, J=8 Hz, 2 Hz), 6.95 (1H, td, J=8 Hz, 2 Hz), 6.87 (1H, dd, J=8 Hz, 1 Hz), 6.79 (1H, t, J=1 Hz), 4.45-4.42 (1H, m), 4.20-4.00 (7H, m), 3.94-3.87 (1H, m), 2.57 (1H, td, J=14 Hz, 4 Hz), 2.50-2.44 (1H, m), 2.18-2.08 (1H, m), 1.85-1.78 (1H, m), 1.45 (3H, t, J=7 Hz), 1.23 (3H, t, J=7 Hz)
##STR00080##
White powder (yield: 48%)
Melting point: 85-88° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.69 (1H, dd, J=8 Hz, 2 Hz), 7.25-7.08 (4H, m), 6.84 (1H, s), 6.57 (1H, dd, J=74 Hz, 73 Hz), 4.44-4.41 (1H, m), 4.21-4.02 (5H, m), 3.95-3.89 (1H, m), 2.57-2.44 (2H, m), 2.21-2.10 (1H, m), 1.90-1.82 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00081##
White powder (yield: 56%)
Melting point: 93-95° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.70 (1H, s), 7.63 (1H, dd, J=8 Hz, 1 Hz), 7.51 (1H, dd, J=8 Hz, 2 Hz), 7.33-7.28 (1H, m), 7.08 (1H, td, J=8 Hz, 1 Hz), 6.82 (1H, q, J=1 Hz), 4.50 (1H, d, J=4 Hz), 4.21-4.01 (5H, m), 3.95-3.88 (1H, m), 2.65-2.50 (2H, m), 2.38 (3H, s), 2.23-2.12 (1H, m), 1.88-1.81 (1H, m), 1.25-1.21 (3H, m).
##STR00082##
Oil (yield: 25%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
11.46 (1H, s), 7.91 (1H, dd, J=8 Hz, 1 Hz), 7.85 (1H, dd, J=8 Hz, 1 Hz), 7.59-7.54 (1H, m), 7.15-7.10 (1H, m), 6.80 (1H, t, J=1 Hz), 4.50-4.47 (1H, m), 4.16-4.00 (5H, m), 3.94-3.88 (1H, m), 2.68-2.59 (4H, m), 2.56-2.49 (1H, m), 2.20-2.09 (1H, m), 1.87-1.80 (1H, m), 1.25 (3H, t, J=7 Hz).
##STR00083##
White powder (yield: 73%)
Melting point: 127-129° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.58 (1H, dd, J=8 Hz, 1 Hz), 7.32-7.13 (8H, m), 6.80 (1H, s), 6.50 (1H, s), 4.36 (1H, dd, J=6 Hz, 2 Hz), 4.23-4.00 (7H, m), 3.93-3.87 (1H, m), 2.36 (1H, td, J=14 Hz, 4 Hz), 2.19-2.13 (1H, m), 2.03-1.94 (1H, m), 1.76-1.70 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00084##
White powder (yield: 71%)
Melting point: 118-121° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.10 (1H, s), 7.58 (1H, dd, J=8 Hz, 2 Hz), 7.23 (1H, dd, J=8 Hz, 2 Hz), 7.20-7.15 (1H, m), 7.07 (1H, td, J=8 Hz, 2 Hz), 6.82 (1H, t, 1 Hz), 4.47-4.44 (1H, m), 4.15-4.00 (5H, m), 3.95-3.85 (5H, m), 2.92-2.83 (4H, m), 2.59-2.50 (2H, m), 2.24-2.12 (1H, m), 1.90-1.82 (1H, m), 1.23 (3H, t, J=7 Hz).
##STR00085##
Pale brown powder (yield: 60%)
Melting point: 156-160° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.78 (1H, d, J=7 Hz), 7.62 (1H, d, J=8 Hz), 7.58 (1H, d, J=7 Hz), 7.54 (1H, d, J=8 Hz), 7.42-7.37 (2H, m), 7.34 (1H, td, J=7 Hz, 1 Hz), 6.92 (1H, s), 6.86 (1H, s), 4.45 (1H, dd, J=6 Hz, 2 Hz), 4.22-4.00 (5H, m), 3.96 (2H, s), 3.94-3.89 (1H, m), 2.56-2.50 (1H, m), 2.37 (1H, td, J=14 Hz, 3 Hz), 2.17-2.08 (1H, m), 1.88-1.82 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00086##
White powder (yield: 26%)
Melting point: 77-80° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
8.50-8.47 (2H, m), 7.54-7.52 (1H, m), 7.26-7.22 (1H, m), 7.19-7.13 (4H, m), 6.89 (1H, t, J=1 Hz), 6.80 (1H, s), 4.43 (1H, dd, J=6 Hz, 3 Hz), 4.25-4.18 (2H, m), 4.14-4.03 (3H, m), 3.96-3.90 (1H, m), 3.15-3.00 (2H, m), 2.99-2.89 (2H, m), 2.54-2.48 (1H, m), 2.33 (1H, td, J=14 Hz, 3 Hz), 2.17-2.09 (1H, m), 1.88-1.82 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00087##
Amorphous substance (yield: 65%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
8.00 (1H, s), 7.62 (1H, d, J=8 Hz), 7.24 (1H, td, J=8 Hz, 2 Hz), 7.17 (1H, d, J=7 Hz), 7.10 (1H, t, J=7 Hz), 6.83 (1H, s), 4.90 (1H, brs), 4.46 (1H, d, J=5 Hz), 4.23-4.01 (5H, m), 3.94-3.88 (1H, m), 3.27 (2H, q, J=7 Hz), 2.96-2.83 (2H, m), 2.59-2.52 (2H, m), 2.18-2.09 (1H, m), 1.83-1.78 (1H, m), 1.48-1.41 (9H, m), 1.27 (3H, t, J=7 Hz).
##STR00088##
Oil (yield: 13%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.39 (1H, dd, J=8 Hz, 2 Hz), 7.11-7.06 (1H, m), 6.89 (1H, t, J=1 Hz), 6.79-6.73 (2H, m), 4.46 (1H, dd, J=6 Hz, 3 Hz), 4.31-3.86 (3H, m), 4.28 (2H, q, J=7 Hz), 4.11-4.02 (3H, m), 3.95-3.89 (1H, m), 2.48-2.41 (1H, m), 2.24 (1H, td, J=14 Hz, 3 Hz), 2.13-2.03 (1H, m), 1.86-1.79 (1H, m), 1.32 (3H, t, J=7 Hz).
##STR00089##
White powder (yield: 74%)
Melting point: 128-131° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.64-7.57 (1H, m), 6.97 (1H, brs), 6.93-6.86 (2H, m), 6.84 (1H, t, J=1 Hz), 4.36 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.02 (5H, m), 3.95-3.90 (1H, m), 2.53-2.46 (1H, m), 2.40 (1H, td, J=1-4 Hz, 4 Hz), 2.21-2.10 (1H, m), 1.88-1.81 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00090##
Pale yellow powder (yield: 48%)
Melting point: 106-111° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9 Hz, 5 Hz), 7.32 (1H, dd, J=8 Hz, 3 Hz), 7.10-7.04 (1H, m), 6.94 (1H, s), 6.82 (1H, t, J=1 Hz), 4.46-4.43 (1H, m), 4.26-4.01 (5H, m), 3.95-3.89 (1H, m), 2.57-2.47 (2H, m), 2.24-2.13 (1H, m), 1.87-1.81 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00091##
White powder (yield: 79%)
Melting point: 103-105° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.85 (3H, m), 6.64 (1H, brs), 4.39 (1H, dd, J=6 Hz, 3 Hz), 4.27-4.18 (2H, m), 4.14-4.02 (3H, m), 3.96-3.89 (1H, m), 2.52-2.45 (1H, m), 2.40-2.31 (4H, m), 2.18-2.08 (1H, m), 1.87-1.80 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00092##
Pale brown powder (yield: 81%)
Melting point: 111-118° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47 (1H, dd, J=6 Hz, 3 Hz), 7.29-7.25 (1H, m), 7.15-7.09 (2H, m), 6.88 (1H, s), 4.28 (2H, q, J=7 Hz), 4.21-4.18 (1H, m), 4.14-4.02 (3H, m), 3.96-3.89 (1H, m), 2.49-2.41 (1H, m), 2.25 (1H, td, J=14 Hz, 3 Hz), 2.12-2.01 (1H, m), 1.89-1.82 (1H, m), 1.34 (3H, t, J=7 Hz).
##STR00093##
White powder (yield: 78%)
Melting point: 109-111° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.64-7.57 (2H, m), 7.27-7.17 (2H, m), 6.89 (1H, s), 4.28 (2H, q, J=7 Hz), 4.19-4.16 (1H, m), 4.14-4.03 (3H, m), 3.96-3.89 (1H, m), 2.49-2.42 (1H, m), 2.26 (1H, td, J=14 Hz, 3 Hz), 2.13-2.03 (1H, m), 1.89-1.83 (1H, m), 1.34 (3H, t, J=7 Hz).
##STR00094##
Oil (yield: 72%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.09 (1H, dd, J=7 Hz, 2 Hz), 7.03 (1H, dd, J=11 Hz, 9 Hz), 6.96 (1H, brs), 6.88-6.83 (2H, m), 4.30-4.23 (3H, m), 4.14-4.02 (3H, m), 3.95-3.89 (4H, m), 2.46-2.38 (1H, m), 2.27 (1H, td, J=14 Hz, 3 Hz), 2.10-2.00 (1H, m), 1.88-1.81 (1H, m), 1.33 (3H, t, J=7 Hz).
##STR00095##
Pale brown powder (yield: 94%)
Melting point: 118-121° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.33-7.26 (1H, m), 7.18-7.06 (3H, m), 6.89 (1H, s), 4.28 (2H, q, J=7 Hz), 4.19 (1H, dd, J=5 Hz, 3 Hz), 4.14-4.02 (3H, m), 3.96-3.89 (1H, m), 2.48-2.41 (1H, m), 2.25 (1H, td, J=14 Hz, 3 Hz), 2.11-2.01 (1H, m), 1.89-1.82 (1H, m), 1.34 (3H, t, J=7 Hz).
##STR00096##
White powder (yield: 49%)
Melting point: 118-121° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47-7.45 (1H, m), 6.78 (2H, d, J=9.8 Hz), 6.50-6.47 (2H, m), 4.38 (1H, d, J=4.7 Hz), 4.21-3.80 (12H, m), 2.54 (1H, dt, J=14.2 Hz, 7.2 Hz), 2.45-2.38 (1H, m), 2.14-2.08 (1H, m), 1.81-1.76 (1H, m), 1.25 (3H, t, J=7.0 Hz).
##STR00097##
Brown oil (yield: 82%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.94 (1H, dd, J=10 Hz, 3 Hz), 6.92-6.86 (2H, m), 6.60 (1H, s), 4.41 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.18 (2H, m), 4.14-4.02 (3H, m), 3.96-3.89 (1H, m), 2.75-2.63 (2H, m), 2.52-2.45 (1H, m), 2.37 (1H, dt, J=14 Hz, 3 Hz), 2.18-2.08 (1H, m), 1.87-1.80 (1H, m), 1.63-1.52 (2H, m), 1.44-1.35 (2H, m), 1.29 (3H, t, J=7 Hz), 0.95 (3H, t, J=8 Hz).
##STR00098##
Brown oil (yield: 78%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.94 (1H, dd, J=10 Hz, 3 Hz), 6.92-6.85 (2H, m), 6.61 (1H, s), 4.40 (1H, dd, J=6 Hz, 2 Hz), 4.27-4.18 (2H, m), 4.14-4.02 (3H, m), 3.95-3.90 (1H, m), 2.76-2.61 (2H, m), 2.52-2.45 (1H, m), 2.37 (1H, dt, J=14 Hz, 3 Hz), 2.18-2.09 (1H, m), 1.87-1.81 (1H, m), 1.65-1.52 (2H, m), 1.39-1.32 (4H, m), 1.30 (3H, t, J=7 Hz), 0.90 (3H, t, J=7 Hz).
##STR00099##
Pale brown oil (yield: 58%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.85 (3H, m), 6.61 (1H, s), 4.40 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.18 (2H, m), 4.14-4.02 (3H, m), 3.95-3.89 (1H, m), 2.76-2.61 (2H, m), 2.52-2.45 (1H, m), 2.37 (1H, td, J=14 Hz, 3 Hz), 2.18-2.08 (1H, m), 1.87-1.81 (1H, m), 1.63-1.52 (2H, m), 1.42-1.25 (9H, m), 0.91-0.85 (3H, m).
##STR00100##
Pale yellow oil (yield: 85%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.87 (3H, m), 6.63 (1H, s), 4.41 (1H, dd, J=6 Hz, 2 Hz), 4.27-4.19 (2H, m), 4.14-3.91 (4H, m), 2.76-2.62 (2H, m), 2.52-2.46 (1H, m), 2.37 (1H, dt, J=14 Hz, 3 Hz), 2.18-2.09 (1H, m), 1.84 (1H, dt, J=13 Hz, 4 Hz), 1.62-1.55 (2H, m), 1.40-1.24 (11H, m), 0.88 (3H, t, J=7 Hz).
##STR00101##
Pale yellow oil (yield: 72%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.87 (3H, m), 6.62 (1H, s), 4.40 (1H, dd, J=6 Hz, 2 Hz), 4.27-4.19 (2H, m), 4.15-3.90 (4H, m), 2.74-2.62 (2H, m), 2.52-2.46 (1H, m), 2.37 (1H, dt, J=14 Hz, 3 Hz), 2.18-2.10 (1H, m), 1.86-1.81 (1H, m), 1.63-1.53 (2H, m), 1.40-1.24 (13H, m), 0.88 (3H, t, J=7 Hz).
##STR00102##
Pale orange oil (yield: 82%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.94 (1H, dd, J=9 Hz, 3 Hz), 6.92-6.85 (2H, m), 6.62 (1H, s), 4.40 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.17 (2H, m), 4.15-4.03 (3H, m), 3.95-3.90 (1H, m), 2.75-2.62 (2H, m), 2.52-2.45 (1H, m), 2.37 (1H, td, J=14 Hz, 3 Hz), 2.18-2.09 (1H, m), 1.86-1.81 (1H, m), 1.63-1.53 (2H, m), 1.39-1.22 (15H, m), 0.88 (3H, t, J=7 Hz).
##STR00103##
Pale yellow oil (yield: 83%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.94 (1H, dd, J=9 Hz, 3 Hz), 6.92-6.85 (2H, m), 6.62 (1H, s), 4.40 (1H, dd, J=5 Hz, 3 Hz), 4.28-4.17 (2H, m), 4.15-4.03 (3H, m), 3.95-3.90 (1H, m), 2.75-2.62 (2H, m), 2.51-2.45 (1H, m), 2.37 (1H, td, J=14 Hz, 3 Hz), 2.18-2.09 (1H, m), 1.86-1.81 (1H, m), 1.63-1.53 (2H, m), 1.39-1.22 (17H, m), 0.88 (3H, t, J=7 Hz).
##STR00104##
White powder (yield: 65%)
Melting point: 130-133° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.62-7.56 (1H, m), 7.18-7.11 (2H, m), 7.02 (1H, s), 6.84 (1H, t, J=1 Hz), 4.37 (1H, dd, J=6 Hz, 2 Hz), 4.25-4.02 (5H, m), 3.96-3.89 (1H, m), 2.55-2.48 (1H, m), 2.42 (1H, td, J=14 Hz, 4 Hz), 2.21-2.11 (1H, m), 1.88-1.82 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00105##
Pale brown powder (yield: 51%)
Melting point: 100-110° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.64 (1H, d, J=9 Hz), 7.56 (1H, d, J=3 Hz), 7.31 (1H, dd, J=9 Hz, 3 Hz), 7.02 (1H, s), 6.83 (1H, t, J=1 Hz), 4.47-4.43 (1H, m), 4.23-4.02 (5H, m), 3.95-3.89 (1H, m), 2.58-2.48 (2H, m), 2.24-2.14 (1H, m), 1.89-1.82 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00106##
White powder (yield: 74%)
Melting point: 123-126° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, d, J=9 Hz), 4.21-4.15 (2H, m), 6.86 (1H, t, J=1 Hz), 6.65 (1H, s), 4.38 (1H, dd, J=6 Hz, 3 Hz), 4.24-4.15 (2H, m), 4.14-4.02 (3H, m), 3.96-3.89 (1H, m), 2.54-2.47 (1H, m), 2.41-2.32 (4H, m), 2.19-2.09 (1H, m), 1.88-1.82 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00107##
White powder (yield: 46%)
Melting point: 131-134° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
10.48 (1H, s), 8.00 (1H, d, J=3 Hz), 7.79 (1H, d, J=9 Hz), 7.50 (1H, dd, J=9 Hz, 3 Hz), 6.80 (1H, t, J=1 Hz), 4.47 (1H, dd, J=6 Hz, 2 Hz), 4.14-4.01 (5H, m), 3.95-3.88 (4H, m), 2.66-2.50 (2H, m), 2.22-2.11 (1H, m), 1.88-1.81 (1H, m), 1.25 (3H, t, J=7 Hz).
##STR00108##
White powder (yield: 66%)
Melting point: 163-164° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, d, J=2 Hz), 7.41 (1H, d, J=9 Hz), 7.23 (1H, dd, J=9 Hz, 3 Hz), 7.16 (1H, s), 6.88 (1H, t, J=1 Hz), 4.27 (2H, q, J=7 Hz), 4.21 (1H, q, J=3 Hz), 4.14-4.02 (3H, m), 3.96-3.88 (1H, m), 2.50-2.43 (1H, m), 2.27 (1H, td, J=14 Hz, 3 Hz), 2.13-2.03 (1H, m), 1.89-1.82 (1H, m), 1.33 (3H, t, J=7 Hz).
##STR00109##
Pale brown powder (yield: 61%)
Melting point: 125-128° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.45-7.41 (1H, m), 7.09-7.00 (2H, m), 6.86 (1H, s), 6.80-6.74 (1H, m), 4.41 (1H, dd, J=6 Hz, 2 Hz), 4.26-4.02 (5H, m), 3.95-3.90 (1H, m), 2.58-2.52 (1H, m), 2.44 (1H, td, J=14 Hz, 3 Hz), 2.23-2.14 (1H, m), 1.89-1.84 (1H, m), 1.28 (3H, t, J=7 Hz).
##STR00110##
White powder (yield: 56%)
Melting point: 129-131° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.25-7.18 (1H, m), 7.01-6.95 (2H, m), 6.89-6.87 (2H, m), 4.64 (1H, dd, J=5 Hz, 2 Hz), 4.31-4.21 (2H, m), 4.15-4.03 (3H, m), 3.96-3.91 (1H, m), 2.63-2.57 (1H, m), 2.36 (1H, td, J=14 Hz, 3 Hz), 2.26-2.17 (1H, m), 1.87-1.82 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00111##
White powder (yield: 69%)
Melting point: 136-138° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.49 (1H, t, J=9 Hz), 6.95-6.92 (2H, m), 6.86 (1H, d, J=2 Hz), 6.83 (1H, s), 4.40-4.37 (1H, m), 4.26-4.15 (2H, m), 4.13-4.01 (3H, m), 3.94-3.89 (1H, m), 2.51-2.40 (2H, m), 2.32 (3H, s), 2.18-2.09 (1H, m), 1.86-1.81 (1H, m), 1.27 (3H, t, J=7 Hz).
##STR00112##
Oil (yield: 63%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.43 (1H, dd, J=8 Hz, 2 Hz), 6.98 (1H, dd, J=10 Hz, 8 Hz), 6.91-6.87 (2H, m), 6.83 (1H, t, J=1 Hz), 4.42 (1H, dd, J=6 Hz, 2 Hz), 4.26-4.02 (5H, m), 3.95-3.89 (1H, m), 2.54-2.42 (2H, m), 2.20-2.12 (1H, m), 1.87-1.82 (1H, m), 1.27 (3H, t, J=7 Hz).
##STR00113##
Pale brown powder (yield: 57%)
Melting point: 167-169° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50 (1H, t, J=9 Hz), 6.82 (1H, t, J=1 Hz), 6.79 (1H, brs), 6.71-6.67 (2H, m), 4.38-4.35 (1H, m), 4.28-4.19 (2H, m), 4.14-4.01 (3H, m), 3.95-3.88 (1H, m), 3.79 (3H, s), 2.49-2.36 (2H, m), 2.18-2.08 (1H, m), 1.86-1.79 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00114##
White powder (yield: 55%)
Melting point: 88-90° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.68-7.65 (1H, m), 7.07-7.01 (3H, m), 6.86 (1H, s), 4.40 (1H, dd, J=6 Hz, 2 Hz), 4.27-4.15 (2H, m), 4.14-4.03 (3H, m), 3.96-3.90 (1H, m), 2.58-2.52 (1H, m), 2.43 (1H, td, J=14 Hz, 3 Hz), 2.23-2.15 (1H, m), 1.89-1.84 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00115##
White powder (yield: 71%)
Melting point: 149-152° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.41-7.34 (1H, m), 7.14 (1H, brs), 7.02-6.93 (1H, m), 6.85 (1H, t, J=1 Hz), 4.36 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.20 (2H, m), 4.14-4.02 (3H, m), 3.96-3.90 (1H, m), 2.55-2.46 (1H, m), 2.38 (1H, td, J=14 Hz, 4 Hz), 2.22-2.12 (1H, m), 1.89-1.82 (1H, m), 1.31 (3H, t, J=7 Hz).
##STR00116##
White powder (yield: 72%)
Melting point: 104-107° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.60-7.52 (1H, m), 7.05-6.97 (2H, m), 6.86 (1H, t, J=1 Hz), 4.35 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.19 (2H, m), 4.15-4.02 (3H, m), 3.96-3.90 (1H, m), 2.56-2.49 (1H, m), 2.38 (1H, td, J=14 Hz, 4 Hz), 2.23-2.12 (1H, m), 1.90-1.83 (1H, m), 1.30 (3H, t, J=7 Hz).
##STR00117##
White powder (yield: 61%)
Melting point: 131-133° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.91 (1H, s), 6.88 (1H, t, J=1 Hz), 6.80-6.72 (2H, m), 4.55 (1H, dd, J=6 Hz, 3 Hz), 4.31-4.23 (2H, m), 4.14-4.03 (3H, m), 3.96-3.90 (1H, m), 2.62-2.55 (1H, m), 2.32 (1H, td, J=14 Hz, 3 Hz), 2.25-2.15 (1H, m), 1.88-1.81 (1H, m), 1.31 (3H, t, J=7 Hz).
##STR00118##
Pale brown powder (yield: 67%)
Melting point: 109-111° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.65 (1H, d, J=9 Hz), 7.41 (1H, d, J=2 Hz), 7.28-7.24 (1H, m), 7.07 (1H, s), 6.83 (1H, s), 4.46-4.42 (1H, m), 4.24-4.02 (5H, m), 3.98-3.89 (1H, m), 2.56-2.46 (2H, m), 2.24-2.13 (1H, m), 1.89-1.82 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00119##
White powder (yield: 74%)
Melting point: 102-107° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.59 (1H, d, J=9 Hz), 7.55 (1H, d, J=2 Hz), 7.40 (1H, dd, J=9 Hz, 2 Hz), 7.08 (1H, s), 6.83 (1H, s), 4.44 (1H, d, J=5 Hz), 4.23-4.02 (5H, m), 3.95-3.89 (1H, m), 2.55-2.47 (2H, m), 2.23-2.14 (1H, m), 1.89-1.83 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00120##
Pale brown powder (yield: 69%)
Melting point: 130-135° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.57 (1H, d, J=9 Hz), 7.20 (1H, d, J=2 Hz), 7.10-7.06 (1H, m), 6.97 (1H, s), 6.81 (1H, d, J=1 Hz), 4.44 (1H, d, J=5 Hz), 4.25-4.00 (5H, m), 3.95-3.87 (1H, m), 2.59-2.45 (2H, m), 2.31 (3H, s), 2.22-2.10 (1H, m), 1.87-1.79 (1H, m), 1.25 (3H, t, J=7 Hz).
##STR00121##
Amorphous substance (yield: 49%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.61 (1H, d, J=9 Hz), 7.38 (1H, d, J=2 Hz), 7.29 (1H, dd, J=9 Hz, 2 Hz), 7.00 (1H, s), 6.82 (1H, s), 4.46 (1H, d, J=4 Hz), 4.23-4.01 (5H, m), 3.95-3.88 (1H, m), 2.59-2.47 (2H, m), 2.23-2.12 (1H, m), 1.87-1.80 (1H, m), 1.29 (9H, s), 1.25-1.21 (3H, m).
##STR00122##
Amorphous substance (yield: 62%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.27-7.24 (1H, m), 7.21-7.15 (1H, m), 7.12-7.06 (1H, m), 6.98 (1H, s), 6.86 (1H, s), 4.77-4.74 (1H, m), 4.30-4.21 (2H, m), 4.15-4.03 (3H, m), 3.96-3.90 (1H, m), 2.67-2.60 (1H, m), 2.38 (1H, td, J=14 Hz, 3 Hz), 2.28-2.17 (1H, m), 1.88-1.81 (1H, m), 1.29 (3H, t, J=7 Hz).
##STR00123##
Amorphous substance (yield: 24%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.39 (1H, s), 7.38 (1H, s), 7.27 (1H, s), 7.17 (1H, t, J=8 Hz), 6.87 (1H, s), 4.88 (1H, dd, J=5 Hz, 3 Hz), 4.29 (2H, q, J=7 Hz), 4.15-4.03 (3H, m), 3.96-3.91 (1H, m), 2.68-2.62 (1H, m), 2.31 (1H, td, J=14 Hz, 3 Hz), 2.26-2.18 (1H, m), 1.88-1.82 (1H, m), 1.31 (3H, t, J=7 Hz).
##STR00124##
Amorphous substance (yield: 55%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.29-7.23 (1H, m), 7.20-7.09 (3H, m), 6.84 (1H, t, J=1 Hz), 4.80-4.77 (1H, m), 4.30-4.20 (2H, m), 4.13-4.00 (3H, m), 3.95-3.89 (1H, m), 2.58-2.46 (4H, m), 2.33 (1H, td, J=14 Hz, 3 Hz), 2.25-2.14 (1H, m), 1.85-1.78 (1H, m), 1.28 (3H, t, J=7 Hz).
##STR00125##
Amorphous substance (yield: 70%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.56-7.61 (1H, m), 7.26-7.19 (3H, m), 5.83 (1H, s), 4.46 (1H, d, J=5 Hz), 4.22-4.01 (5H, m), 3.95-3.89 (1H, m), 2.57-2.48 (2H, m), 2.25-2.14 (1H, m), 1.89-1.82 (1H, m), 1.25 (3H, t, J=7 Hz).
##STR00126##
White powder (yield: 78%)
Melting point: 120-124° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.72 (1H, d, J=2 Hz), 7.31 (1H, d, J=9 Hz), 7.11 (1H, s), 7.05 (1H, dd, J=9 Hz, 2 Hz), 6.86 (1H, s), 4.46 (1H, dd, J=6 Hz, 2 Hz), 4.25-4.03 (5H, m), 3.95-3.90 (1H, m), 2.58-2.48 (2H, m), 2.26-2.17 (1H, m), 1.90-1.84 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00127##
Oil (yield: 29%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.07-7.03 (1H, m), 6.99 (1H, s), 6.91-6.83 (2H, m), 4.67 (1H, dd, J=5 Hz, 3 Hz), 4.31-4.23 (2H, m), 4.14-4.03 (3H, m), 3.97-3.90 (1H, m), 2.65-2.57 (1H, m), 2.34 (1H, td, J=14 Hz, 3 Hz), 2.27-2.17 (1H, m), 1.88-1.81 (1H, m), 1.31 (3H, t, J=7 Hz).
##STR00128##
Amorphous substance (yield: 39%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.22 (1H, s), 7.17 (2H, d, J=7 Hz), 6.88 (1H, t, J=1 Hz), 4.84-4.81 (1H, m), 4.29 (2H, q, J=7 Hz), 4.14-4.03 (3H, m), 3.97-3.90 (1H, m), 2.67-2.60 (1H, m), 2.34-2.17 (2H, m), 1.88-1.81 (1H, m), 1.33 (3H, t, J=7 Hz).
##STR00129##
Amorphous substance (yield: 46%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.35 (1H, dd, J=7.5 Hz, 2.8 Hz), 7.24-7.21 (2H, m), 7.24 (1H, s), 4.90 (1H, d, J=5.1 Hz), 4.30 (2H, q, J=7.2 Hz), 4.14-3.92 (4H, m), 2.67-2.62 (1H, m), 2.33-2.18 (2H, m), 1.88-1.84 (1H, m), 1.33 (3H, t, J=6.6 Hz).
##STR00130##
White powder (yield: 54%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.43 (1H, s), 6.96 (1H, s), 6.87 (1H, s), 6.78 (1H, t, J=1 Hz), 4.41 (1H, dd, J=6 Hz, 2 Hz), 4.20-4.00 (5H, m), 3.94-3.88 (1H, m), 3.85 (3H, s), 2.58-2.43 (2H, m), 2.31 (3H, s), 2.20-2.08 (1H, m), 1.85-1.78 (1H, m), 1.25 (3H, t, J=7 Hz).
##STR00131##
Oil (yield: 56%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.70 (1H, d, J=2 Hz), 7.59 (1H, d, J=9 Hz), 7.44 (1H, dd, J=9 Hz, 2 Hz), 7.02 (1H, s), 6.83 (1H, s), 4.47-4.44 (1H, m), 4.23-4.02 (5H, m), 3.95-3.90 (1H, m), 2.57-2.49 (2H, m), 2.23-2.15 (1H, m), 1.88-1.83 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00132##
Amorphous substance (yield: 41%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.61 (2H, d, J=8 Hz), 7.26 (1H, brs), 7.02 (1H, t, J=8 Hz), 6.88 (1H, s), 5.02-5.00 (1H, m), 4.29 (2H, q, J=7 Hz), 4.15-3.91 (4H, m), 2.70-2.64 (1H, m), 2.33-2.19 (2H, m), 1.87-1.83 (1H, m), 1.32 (3H, t, J=7 Hz).
##STR00133##
White powder (yield: 51%)
Melting point: 130-134° C.
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.60 (1H, d, J=8 Hz), 7.40 (1H, d, J=2 Hz), 7.18 (1H, dd, J=8 Hz, 2 Hz), 6.94 (1H, s), 6.82 (1H, s), 4.48-4.46 (1H, m), 4.24-4.01 (5H, m), 3.94-3.88 (1H, m), 2.89-2.83 (1H, m), 2.60-2.47 (2H, m), 2.22-2.13 (1H, m), 1.86-1.81 (1H, m), 1.25-1.21 (9H, m).
##STR00134##
Ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 1 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white powder. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 1:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 6.1 minutes
high polarity compound (second peak): 10.5 minutes
(Low Polarity Compound, First Peak)
Melting point: 116-117° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9.2 Hz, 5.3 Hz), 7.17 (1H, dd, J=7.8 Hz, 2.7 Hz), 7.05-7.00 (2H, m), 6.83 (1H, s), 4.43 (1H, d, J=5.4 Hz), 4.26-3.90 (6H, m), 2.55-2.47 (2H, m), 4.15-2.47 (1H, m), 4.02-2.13 (1H, m), 1.27 (3H, t, J=7.0 Hz).
(High Polarity Compound, Second Peak)
Melting point: 116-117° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9.0 Hz, 5.5 Hz), 7.17 (1H, dd, J=8.0 Hz, 2.9 Hz), 7.06-7.00 (2H, m), 6.84 (1H, s), 4.43 (1H, d, J=5.4 Hz), 4.26-3.90 (6H, m), 2.55-2.47 (2H, m), 1.13-2.23 (1H, m), 1.87-1.83 (1H, m), 1.27 (3H, t, J=6.6 Hz).
##STR00135##
Following the process described in Example (30e), ethyl 7-oxo-1,4-dioxaspiro[4.5]decane-8-carboxylate [compound disclosed as Compound 292c in US Patent application No. US2004/259914 A1] was used in place of ethyl 8-oxo-1-oxaspiro[4.5]decane-7-carboxylate to give the title compound as a white powder (yield: 96%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.28 (2H, q, J=7 Hz), 4.04-3.96 (4H, m), 2.65-2.61 (4H, m), 1.82-1.78 (2H, m), 1.32 (3H, t, J=7 Hz).
Following the process described in Example (1a), ethyl 7-trifluoromethanesulfonyloxy-1,4-dioxaspiro[4.5]dec-7-ene-8-carboxylate obtained in (123a) was used in place of ethyl 8-trifluoromethanesulfonyloxy-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to obtain the title compound as a pale brown oil (yield: 83%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.21 (2H, q, 7 Hz), 4.04-3.96 (4H, m), 2.72-2.65 (4H, m), 2.32 (3H, s), 1.85 (2H, t, J=7 Hz), 1.29 (3H, t, J=7 Hz).
Following the process described in Example (1b), ethyl 7-acetylsulfanyl-1,4-dioxaspiro[4.5]dec-7-ene-8-carboxylate obtained in (123b) was used in place of ethyl 8-acetylsulfanyl-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to give the title compound as a pale brown powder (yield: 85%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.22 (2H, q, 7 Hz), 4.20 (1H, s), 4.02-3.95 (4H, m), 2.69-2.66 (2H, m), 2.61-2.56 (2H, m), 1.82-1.78 (2H, m), 1.30 (3H, t, J=7 Hz).
Following the process described in Example (1c), ethyl 7-mercapto-1,4-dioxaspiro[4.5]dec-7-ene-8-carboxylate obtained in (123c) was used in place of ethyl 8-mercapto-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to give the title compound as a colorless oil (yield: 62%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.31 (2H, q, 7 Hz), 4.09-4.00 (4H, m), 2.82-2.73 (4H, m), 1.86 (2H, t, J=7 Hz), 1.35 (3H, t, J=7 Hz).
Following the process described in Example (1d), ethyl 7-chlorosulfonyl-1,4-dioxaspiro[4.5]dec-7-ene-8-carboxylate obtained in (123d) was used in place of ethyl 8-chlorosulfonyl-1,4-dioxaspiro[4.5]dec-7-ene-7-carboxylate to give the title compound as a white powder (yield: 61%).
Melting point: 120-122° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.81 (1H, s), 7.66 (1H, dd, J=9 Hz, 5 Hz), 7.14-7.10 (2H, m), 6.98-6.92 (1H, m), 4.71-4.67 (1H, m), 4.22-3.96 (6H, m), 2.75-2.56 (3H, m), 2.08-2.02 (1H, m), 1.24 (3H, t, J=7 Hz).
##STR00136##
Following the process described in Example (17a), 1-bromo-2,3-bis[(trimethylsilyl)oxy]propane was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a white amorphous substance (yield: 100%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9.2 and 5.3 Hz), 7.17 (1H, dd, J=7.8 and 2.8 Hz), 7.05-6.99 (2H, m), 6.86-6.77 (1H, m), 4.53-3.84 (6H, m), 3.53-3.31 (2H, m), 2.66-2.41 (2H, m), 2.24-2.12 (1H, m), 1.89-1.86 (1H, m), 1.28-1.24 (3H, m).
##STR00137##
Following the process described in Example (17a), methyl (S)-3,4-bis[(trimethylsilyl)oxy]butyrate obtained in Reference Example 20 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a colorless oil (yield: 96%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9.0 Hz, 5.4 Hz), 7.16 (1H, dd, J=7.9 Hz, 2.8 Hz), 7.05-6.98 (2H, m), 6.88-6.76 (1H, m), 4.63-4.58 (1H, m), 4.47-4.41 (1H, m), 4.32-4.10 (3H, m), 3.84-3.59 (4H, m), 2.85-2.39 (4H, m), 2.21-2.16 (1H, m), 1.89-1.80 (1H, m), 1.29-1.24 (3H, m).
##STR00138##
34 mg (0.61 mmol) of 1,4-butanediol was dissolved in 5 ml of dichloromethane, 0.32 ml (1.83 mmol) of isopropoxytrimethylsilane, and 200 mg (0.47 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) and 4 μl (0.024 mmol) of trimethylsilyl trifluoromethanesulfonate were sequentially added thereto with stirring under ice-cooling, followed by stirring for 2 hours at the same temperature. Saturated aqueous sodium hydrogencarbonate was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1), and the resulting solid was further washed with hexane to give 6 mg of the title compound as a white powder (yield: 3%).
Melting point: 142-144° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9 Hz, 5 Hz), 7.16 (1H, dd, J=8 Hz, 3 Hz), 7.04 (1H, s), 7.03-6.98 (2H, m), 4.44-4.40 (1H, m), 4.27-4.11 (2H, m), 3.91-3.62 (4H, m), 2.46-2.38 (1H, m), 2.31-2.21 (1H, m), 2.17-1.94 (2H, m), 1.71-1.58 (4H, m), 1.27 (3H, t, J=7 Hz).
##STR00139##
Following the process described in Example 21, 1,4-anhydro-2,3-di-O-trimethylsilyl-meso-erythritol obtained in Reference Example 21 was used in place of 1,3,4,5,7-penta-O-trimethylsilyl-D-arabitol to give the title compound as a white powder (yield: 56%).
Melting point: 227-228° C.
1H-NMR spectrum (400 MHz, CDCl3+CD3OD) δ ppm:
7.61 (1H, dd, J=9 Hz, 5 Hz), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.07-6.97 (1H, m), 6.91 (1H, s), 4.93 (1H, dd, J=6 Hz, 4 Hz), 4.81 (1H, dd, J=6 Hz, 4 Hz), 4.39 (1H, d, J=5 Hz), 4.26-4.05 (3H, m), 4.01 (1H, d, J=11 Hz), 3.51-3.41 (2H, m), 2.54-2.34 (2H, m), 2.20-2.07 (1H, m), 1.90-1.79 (1H, m), 1.25 (3H, t, J=7 Hz).
##STR00140##
Following the process described in Example (17a), 2,3-dimethyl-2,3-bis[(trimethylsilyl)oxy]butane was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a pale yellow oil (yield: 10%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=8.8 Hz, 5.6 Hz), 7.16 (1H, dd, J=7.8 Hz, 2.7 Hz), 7.04-7.03 (1H, m), 6.89 (1H, s), 4.37 (1H, d, J=4.0 Hz), 4.25-4.10 (2H, m), 2.51-2.43 (2H, m), 2.24-2.14 (1H, m), 1.94-1.89 (1H, m), 1.31-1.23 (15H, m).
##STR00141##
Following the process described in Example (17a), 3-ethyl-3,4-bis[(trimethylsilyl)oxy]hexane obtained in Reference Example 22 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a white powder (yield: 88%).
Melting point: 124-126° C.
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.69-7.66 (1H, m), 7.17-7.15 (1H, m), 7.04-7.00 (2H, m), 6.88-6.69 (1H, m), 4.40-4.39 (1H, m), 4.28-4.10 (2H, m), 3.90-3.68 (1H, m), 2.54-2.31 (2H, m), 2.25-2.12 (1H, m), 1.85-1.37 (7H, m), 1.29-1.24 (3H, m), 1.08-0.84 (9H, m).
##STR00142##
Following the process described in Example (17a), (R)-1,2-bis[(trimethylsilyl)oxy]-1,1,2-triphenylethane obtained in Reference Example 23 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a colorless oil (yield: 30%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.22-6.91 (20H, m), 5.99-5.76 (1H, m), 4.54-4.32 (1H, m), 4.34-4.08 (2H, m), 2.87-1.97 (4H, m), 1.36-1.14 (3H, m).
##STR00143##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-chlorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 54 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 31%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.71-7.67 (1H, m), 7.41-7.38 (1H, m), 7.32-7.26 (1H, m), 7.14-7.06 (2H, m), 6.90 (0.5H, t, J=1 Hz), 6.84 (0.5H, t, J=1 Hz), 4.47 (1H, dd, J=6 Hz, 2 Hz), 4.26-4.07 (3.5H, m), 4.05-4.00 (0.5H, m), 3.94-3.80 (2H, m), 3.77-3.67 (2H, m), 2.64-2.47 (2H, m), 2.27-1.87 (4H, m), 1.27-1.22 (3H, m).
##STR00144##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-bromophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 55 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 28%)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.71-7.67 (1H, m), 7.56 (1H, d, J=8 Hz), 7.35-7.31 (1H, m), 7.07-6.98 (2H, m), 6.90 (0.5H, s), 6.84 (0.5H, s), 4.48 (1H, d, J=5 Hz), 4.25-4.08 (3.5H, m), 4.06-4.01 (0.5H, m), 3.94-3.80 (2H, m), 3.76-3.68 (2H, m), 2.65-2.48 (2H, m), 2.23-1.87 (4H, m), 1.27-1.22 (3H, m).
##STR00145##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-iodophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 56 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 26%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.80 (1H, d, J=8 Hz), 7.68-7.63 (1H, m), 7.38-7.33 (1H, m), 6.90-6.83 (3H, m), 4.50-4.46 (1H, m), 4.27-4.09 (3.5H, m), 4.06-4.02 (0.5H, m), 3.94-3.80 (2H, m), 3.77-3.68 (2H, m), 3.53 (1H, brs), 2.66-2.56 (1H, m), 2.55-2.49 (1H, m), 2.24-2.14 (1H, m), 2.00-1.85 (2H, m), 1.27-1.23 (3H, m).
##STR00146##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-hexylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 4 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a colorless oil (yield: 28%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.54-7.50 (1H, m), 7.23-7.17 (2H, m), 7.15-7.09 (1H, m), 6.94-6.91 (0.5H, m), 6.88-6.85 (0.5H, m), 6.70 (0.5H, s), 6.65 (0.5H, s), 4.48-4.43 (1H, m), 4.28-4.08 (3.5H, m), 4.06-4.00 (0.5H, m), 3.93-3.80 (2H, m), 3.76-3.68 (2H, m), 2.70-2.61 (2H, m), 2.55-2.41 (2H, m), 2.21-2.07 (1H, m), 1.96-1.75 (3H, m), 1.64-1.52 (2H, m), 1.42-1.23 (9H, m), 0.91-0.85 (3H, m).
##STR00147##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-heptylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 5 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a colorless oil (yield: 33%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.54-7.50 (1H, m), 7.23-7.18 (2H, m), 7.14-7.09 (1H, m), 6.94-6.91 (0.5H, m), 6.88-6.85 (0.5H, m), 6.70 (0.5H, s), 6.65 (0.5H, s), 4.47-4.43 (1H, m), 4.28-4.08 (3.5H, m), 4.06-4.00 (0.5H, m), 3.93-3.80 (2H, m), 3.76-3.68 (2H, m), 2.70-2.61 (2H, m), 2.54-2.41 (2H, m), 2.20-2.08 (1H, m), 1.96-1.74 (3H, m), 1.64-1.53 (2H, m), 1.41-1.22 (11H, m), 0.88 (3H, t, J=7 Hz).
##STR00148##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-chloro-4-methylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 108 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 50%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.56 (1H, dd, J=8 Hz, 2 Hz), 7.23-7.21 (1H, m), 7.11-7.07 (1H, m), 7.01 (1H, brs), 6.90 (0.5H, t, J=1 Hz), 6.84-6.82 (0.5H, m), 4.44 (1H, dd, J=6 Hz, 2 Hz), 4.27-4.08 (3.5H, m), 4.05-4.00 (0.5H, m), 3.93-3.80 (2H, m), 3.77-3.68 (2H, m), 2.63-2.44 (2H, m), 2.31 (3H, s), 2.22-1.62 (4H, m), 1.29-1.23 (3H, m).
##STR00149##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2,4-dichlorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 106 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 22%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.64 (1H, dd, J=9 Hz, 2 Hz), 7.41 (1H, d, J=2 Hz), 7.28-7.25 (1H, m), 7.07 (1H, brs), 6.91 (0.5H, t, J=1 Hz), 6.85 (0.5H, t, J=1 Hz), 4.43 (1H, dd, J=6 Hz, 2 Hz), 4.26-4.09 (3.5H, m), 4.07-4.02 (0.5H, m), 3.94-3.81 (2H, m), 3.77-3.68 (2H, m), 2.60-2.47 (2H, m), 2.24-1.85 (4H, m), 1.29-1.24 (3H, m).
##STR00150##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-bromo-4-chlorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 93 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 10%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.64 (1H, dd, J=9 Hz, 3 Hz), 7.57 (1H, d, J=2 Hz), 7.31 (1H, dd, J=9 Hz, 2 Hz), 7.01 (1H, brs), 6.91 (0.5H, s), 6.85 (0.5H, s), 4.45 (1H, d, J=4 Hz), 4.26-4.10 (3.5H, m), 4.06-4.02 (0.5H, m), 3.94-3.82 (2H, m), 3.77-3.69 (2H, m), 2.61-2.48 (2H, m), 2.24-2.15 (1H, m), 2.02-1.85 (3H, m), 1.29-1.24 (3H, m).
##STR00151##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-chloro-6-methylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 112 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 45%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.28 (1H, dd, J=8 Hz, 1 Hz), 7.23-7.07 (3H, m), 6.93-6.91 (0.5H, m), 6.86-6.85 (0.5H, m), 4.80-4.76 (1H, m), 4.30-4.17 (3H, m), 4.11-4.07 (0.5H, m), 4.04-4.00 (0.5H, m), 3.92-3.81 (2H, m), 3.75-3.69 (2H, m), 2.59-2.48 (3H, m), 2.42-2.33 (1H, m), 2.26-2.15 (1H, m), 2.07 (1H, brs), 1.94-1.85 (1H, m), 1.63 (1H, brs), 1.29-1.24 (3H, m).
##STR00152##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(3-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 80 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 47%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47 (1H, dd, J=6 Hz, 3 Hz), 7.29-7.25 (1H, m), 7.17-7.06 (2H, m), 6.97 (0.5H, t, J=1 Hz), 6.93-6.92 (0.5H, m), 4.33-4.09 (4.5H, m), 4.06-4.02 (0.5H, m), 3.94-3.82 (2H, m), 3.77-3.68 (2H, m), 2.48-2.40 (1H, m), 2.34-2.24 (1H, m), 2.12-2.01 (2H, m), 1.97-1.89 (2H, m), 1.35 (3H, t, J=7 Hz).
##STR00153##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-chloro-4,6-difluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 115 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 35%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.07-6.85 (4H, m), 4.67 (1H, dd, J=10 Hz, 6 Hz), 4.32-4.19 (3H, m), 4.14-4.02 (1H, m), 3.93-3.82 (2H, m), 3.76-3.70 (2H, m), 2.66-2.55 (1H, m), 2.43-2.34 (1H, m), 2.28-2.17 (1H, m), 2.06-1.88 (3H, m), 1.33-1.29 (3H, m).
##STR00154##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2,6-dichloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 116 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 25%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.26-7.05 (3H, m), 6.97-6.95 (0.5H, m), 6.90-6.89 (0.5H, m), 4.85-4.80 (1H, m), 4.33-4.19 (3H, m), 4.13-4.08 (0.5H, m), 4.06-4.02 (0.5H, m), 3.93-3.82 (2H, m), 3.76-3.70 (2H, m), 2.72-2.56 (1H, m), 2.39-2.20 (2H, m), 2.05-1.59 (3H, m), 1.35-1.30 (3H, m).
##STR00155##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-bromo-6-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 117 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 29%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.36-7.31 (1H, m), 7.23-7.19 (1H, m), 7.16 (1H, brs), 6.95 (0.5H, s), 6.90-6.88 (0.5H, m), 4.91-4.85 (1H, m), 4.33-4.17 (3H, m), 4.15-4.00 (1H, m), 3.94-3.80 (2H, m), 3.76-3.70 (2H, m), 3.55 (1H, brs), 2.70-2.57 (1H, m), 2.38-2.16 (2H, m), 1.96-1.87 (2H, m), 1.35-1.30 (3H, m).
##STR00156##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2,4-difluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 77 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 35%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.63-7.56 (1H, m), 7.07 (1H, brs), 6.94-6.85 (3H, m), 4.38-4.34 (1H, m), 4.30-4.08 (3.5H, m), 4.06-4.00 (0.5H, m), 3.93-3.81 (2H, m), 3.78-3.68 (2H, m), 2.53-2.40 (2H, m), 2.38-1.87 (4H, m), 1.31-1.27 (3H, m).
##STR00157##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(2,4-difluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 77 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 58%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.62-7.57 (1H, m), 6.93-6.86 (3H, m), 4.37-4.34 (1H, m), 4.29-4.18 (3H, m), 4.13-4.09 (0.5H, m), 4.06-4.01 (0.5H, m), 3.94-3.82 (2H, m), 3.76-3.69 (2H, m), 2.53-2.39 (2H, m), 2.21-1.50 (4H, m), 1.32-1.27 (3H, m).
##STR00158##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 78 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 33%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.69-7.64 (1H, m), 7.33 (1H, dd, J=7 Hz, 3 Hz), 7.10-7.05 (1H, m), 6.93 (1H, brs), 6.93 (0.5H, s), 6.84 (0.5H, s), 4.44 (1H, d, J=4 Hz), 4.27-4.09 (3.5H, m), 4.06-4.01 (0.5H, m), 3.94-3.80 (2H, m), 3.77-3.68 (2H, m), 3.54 (1H, brs), 2.61-2.46 (2H, m), 2.23-2.14 (1H, m), 2.02-1.85 (2H, m), 1.29-1.24 (3H, m).
##STR00159##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 78 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a white amorphous substance (yield: 49%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.69-7.65 (1H, m), 7.33 (1H, dd, J=8 Hz, 3 Hz), 7.10-7.06 (1H, m), 6.99 (1H, brs), 6.91 (0.5H, s), 6.83 (0.5H, s), 4.44 (1H, d, J=4 Hz), 4.24-3.73 (8H, m), 2.61-2.48 (2H, m), 2.61-2.48 (1H, m), 1.96-1.87 (1H, m), 1.26 (3H, t, J=6 Hz).
##STR00160##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 85 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a pale red amorphous substance (yield: 40%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.51-7.45 (1H, m), 6.97-6.85 (3H, m), 6.65 (0.5H, s), 6.59 (0.5H, s), 4.43-4.36 (1H, m), 4.29-4.16 (3H, m), 4.13-4.08 (0.5H, m), 4.07-4.01 (0.5H, m), 3.95-3.80 (2H, m), 3.77-3.68 (2H, m), 2.78-2.62 (2H, m), 2.53-2.35 (2H, m), 2.19-1.84 (4H, m), 1.65-1.49 (2H, m), 1.44-1.35 (2H, m), 1.33-1.27 (3H, m), 0.95 (3H, t, J=7 Hz).
##STR00161##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 85 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a pale red amorphous substance (yield: 14%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.44 (1H, m), 6.98-6.86 (3H, m), 6.73 (0.4H, s), 6.68 (0.6H, s), 4.43-4.37 (1H, m), 4.26-4.16 (3H, m), 4.11-4.07 (0.4H, m), 4.05-3.99 (0.6H, m), 3.90-3.80 (2H, m), 3.78-3.68 (2H, m), 2.77-2.62 (2H, m), 2.53-2.23 (3H, m), 2.20-2.07 (2H, m), 1.96-1.86 (1H, m), 1.63-1.53 (2H, m), 1.44-1.34 (2H, m), 1.32-1.26 (3H, m), 0.95 (3H, t, J=7 Hz).
##STR00162##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 86 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a pale red amorphous substance (yield: 33%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.43 (1H, m), 6.97-6.85 (3H, m), 6.67 (0.5H, s), 6.61 (0.5H, s), 4.42-4.37 (1H, m), 4.30-4.17 (3H, m), 4.12-4.08 (0.5H, m), 4.05-4.01 (0.5H, m), 3.93-3.82 (2H, m), 3.76-3.68 (2H, m), 2.77-2.61 (2H, m), 2.53-2.35 (2H, m), 2.19-1.80 (4H, m), 1.66-1.50 (2H, m), 1.40-1.22 (7H, m), 0.95-0.87 (3H, m).
##STR00163##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 86 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a pale red amorphous substance (yield: 30%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.42 (1H, m), 6.97-6.84 (3H, m), 6.77 (0.5H, s), 6.72 (0.5H, s), 4.42-4.36 (1H, m), 4.30-4.14 (3H, m), 4.12-4.05 (0.5H, m), 4.04-3.98 (0.5H, m), 3.91-3.77 (2H, m), 3.76-3.67 (2H, m), 2.76-2.59 (2H, m), 2.53-2.20 (4H, m), 2.20-2.06 (1H, m), 1.97-1.84 (1H, m), 1.66-1.52 (2H, m), 1.41-1.22 (7H, m), 0.95-0.88 (3H, m).
##STR00164##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 87 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 54%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.45 (1H, m), 6.96-6.86 (3H, m), 6.67 (0.5H, s), 6.61 (0.5H, s), 4.41-4.37 (1H, m), 4.30-4.16 (3H, m), 4.13-4.08 (0.5H, m), 4.06-4.01 (0.5H, m), 3.93-3.81 (2H, m), 3.76-3.69 (2H, m), 2.76-2.61 (2H, m), 2.52-2.36 (2H, m), 2.20-1.50 (6H, m), 1.41-1.26 (9H, m), 0.91-0.85 (3H, m).
##STR00165##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 87 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 54%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.44 (1H, m), 6.96-6.86 (3H, m), 6.70-6.67 (0.5H, m), 6.64-6.61 (0.5H, m), 4.41-4.37 (1H, m), 4.29-4.15 (3H, m), 4.12-4.07 (0.5H, m), 4.05-4.00 (0.5H, m), 3.93-3.80 (2H, m), 3.76-3.68 (2H, m), 2.76-2.61 (2H, m), 2.52-2.35 (2H, m), 2.31-1.51 (6H, m), 1.40-1.26 (9H, m), 0.91-0.86 (3H, m).
##STR00166##
Following the process described in Example 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(4-fluoro-2-heptylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 88 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 41%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, m), 6.96-6.87 (3H, m), 6.68 (0.5H, s), 6.61 (0.5H, s), 4.41-4.40 (1H, m), 4.30-3.71 (8H, m), 2.72-2.65 (2H, m), 2.48-2.39 (2H, m), 2.14-2.10 (2H, m), 1.95-1.87 (2H, m), 1.37-1.22 (11H, m), 0.88 (3H, t, J=7 Hz).
##STR00167##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-heptylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 88 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a white amorphous substance (yield: 70%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50, 7.48 (1H, m), 6.97-6.88 (3H, m), 6.70 (0.5H, s), 6.70 (0.5H, s), 4.41-4.39 (1H, m), 4.28-3.71 (8H, m), 2.75-2.63 (2H, m), 2.51-2.37 (2H, m), 2.19-2.10 (2H, m), 1.95-1.88 (2H, m), 1.35-1.23 (11H, m), 0.88 (3H, t, J=7 Hz).
##STR00168##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(4-fluoro-2-octylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 89 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 47%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.51-7.47 (1H, m), 6.97-6.88 (3H, m), 6.71 (0.5H, s), 6.64 (0.5H, s), 4.41-4.39 (1H, m), 4.28-3.72 (8H, m), 2.76-2.62 (2H, m), 2.51-2.37 (2H, m), 2.18-1.89 (4H, m), 1.37-1.27 (13H, m), 0.88 (3H, t, J=7 Hz).
##STR00169##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-octylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 89 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 51%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.88 (3H, m), 6.69 (0.5H, s), 6.63 (0.5H, s), 4.41-4.39 (1H, m), 4.31-3.70 (8H, m), 2.72-2.66 (2H, m), 2.52-2.37 (2H, m), 2.19-1.88 (4H, m), 1.37-1.27 (13H, m), 0.88 (3H, t, J=7 Hz).
##STR00170##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(4-fluoro-2-nonylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 90 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 48%). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 4.43 minutes
high polarity compound (second peak): 4.73 minutes
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.45 (1H, m), 6.97-6.86 (3H, m), 6.66 (0.5H, s), 6.60 (0.5H, s), 4.42-4.37 (1H, m), 4.28-4.18 (3H, m), 4.13-4.08 (0.5H, m), 4.06-4.01 (0.5H, m), 3.95-3.81 (2H, m), 3.76-3.69 (2H, m), 2.77-2.61 (2H, m), 2.53-2.35 (2H, m), 2.19-1.99 (2H, m), 1.96-1.86 (2H, m), 1.64-1.52 (2H, m), 1.40-1.18 (15H, m), 0.91-0.85 (3H, m).
##STR00171##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-nonylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 90 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 54%). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 6.7 minutes
high polarity compound (second peak): 10.1 minutes
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.50-7.45 (1H, m), 6.97-6.86 (3H, m), 6.71 (0.5H, s), 6.65 (0.5H, s), 4.42-4.37 (1H, m), 4.30-4.16 (3H, m), 4.13-4.08 (0.5H, m), 4.05-4.00 (0.5H, m), 3.93-3.80 (2H, m), 3.77-3.69 (2H, m), 2.76-2.61 (2H, m), 2.52-2.01 (5H, m), 1.95-1.86 (1H, m), 1.64-1.52 (2H, m), 1.41-1.22 (15H, m), 0.88 (3H, t, J=7 Hz).
##STR00172##
Following the process described in Examples 7, (16a) and 17 (alternative procedure), ethyl 8-[N-(2-decyl-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 91 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 35%). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 4.30 minutes
high polarity compound (second peak): 4.55 minutes
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.51-7.45 (1H, m), 6.97-6.86 (3H, m), 6.67 (0.5H, s), 6.61 (0.5H, s), 4.42-4.36 (1H, m), 4.30-4.17 (3H, m), 4.13-4.08 (0.5H, m), 4.06-4.01 (0.5H, m), 3.94-3.80 (2H, m), 3.76-3.69 (2H, m), 2.76-2.61 (2H, m), 2.53-2.35 (2H, m), 2.19-2.00 (2H, m), 1.99-1.86 (2H, m), 1.65-1.51 (2H, m), 1.40-1.18 (17H, m), 0.91-0.85 (3H, m).
##STR00173##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(2-decyl-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 91 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 56%). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 6.4 minutes
high polarity compound (second peak): 9.1 minutes
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.50-7.45 (1H, m), 6.97-6.87 (3H, m), 6.70 (0.5H, s), 6.64 (0.5H, s), 4.42-4.38 (1H, m), 4.30-4.17 (3H, m), 4.12-4.08 (0.5H, m), 4.05-4.01 (0.5H, m), 3.93-3.81 (2H, m), 3.78-3.69 (2H, m), 2.76-2.62 (2H, m), 2.52-2.37 (2H, m), 2.33-2.09 (2H, m), 2.06-1.87 (2H, m), 1.63-1.52 (2H, m), 1.40-1.22 (17H, m), 0.88 (3H, t, J=7 Hz).
##STR00174##
Ethyl (2R,3R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 17 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 12.0 minutes
high polarity compound (second peak): 16.5 minutes
(Low Polarity Compound, First Peak)
Optical rotation [α]D+86.7 (c=2.0, MeOH)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.07-6.98 (2H, m), 6.91 (1H, s), 4.42 (1H, dd, J=6 Hz, 2 Hz), 4.28-4.08 (4H, m), 3.91 (1H, dd, J=12 Hz, 4 Hz), 3.84 (1H, dd, J=12 Hz, 4 HZ), 3.77-3.68 (2H, m), 2.60-2.43 (2H, m), 2.26-2.11 (1H, m), 1.99-1.87 (1H, m), 1.58 (2H, bs), 1.27 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=9 Hz, 5 Hz), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.07-6.98 (2H, m), 6.84 (1H, s), 4.42 (1H, d, J=5 Hz), 4.28-4.08 (3H, m), 4.07-4.01 (1H, m), 3.93-3.82 (2H, m), 3.77-3.68 (2H, m), 2.61-2.46 (2H, m), 2.24-2.11 (1H, m), 1.95-1.87 (1H, m), 1.57 (2H, bs), 1.27 (3H, t, J=7 Hz).
##STR00175##
Ethyl (2S,3S)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 18 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 11.4 minutes
high polarity compound (second peak): 27.4 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=9 Hz, 5 Hz), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.06-7.00 (1H, m), 6.98 (1H, s), 6.84 (1H, s), 4.42 (1H, d, J=5 Hz), 4.27-4.09 (3H, m), 4.07-4.00 (1H, m), 3.93-3.83 (2H, m), 3.76-3.68 (2H, m), 2.60-2.47 (2H, m), 2.24-2.12 (1H, m), 1.95-1.60 (3H, m), 1.27 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.06-6.99 (2H, m), 6.90 (1H, s), 4.44-4.41 (1H, m), 4.27-4.09 (4H, m), 3.91 (1H, dd, J=12 Hz, 4 Hz), 3.84 (1H, dd, J=12 Hz, 4 HZ), 3.77-3.68 (2H, m), 2.60-2.45 (2H, m), 2.24-2.12 (1H, m), 2.00-1.65 (3H, m), 1.27 (3H, t, J=7 Hz).
##STR00176##
Ethyl (2R,3R)-8-[N-(2,4-difluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 144 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as an amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 13.7 minutes
high polarity compound (second peak): 15.9 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.62-7.57 (1H, m), 6.93-6.87 (3H, m), 4.36 (1H, q, J=3 Hz), 4.28-4.18 (3H, m), 4.15-4.09 (1H, m), 3.91 (1H, dd, J=12 Hz, 4 Hz), 3.84 (1H, dd, J=12 Hz, 4 Hz), 3.75-3.70 (2H, m), 2.51-2.40 (2H, m), 2.20-2.12 (1H, m), 1.96-1.90 (1H, m), 1.61 (2H, brs), 1.29 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.62-7.57 (1H, m), 6.97 (1H, brs), 6.93-6.86 (3H, m), 4.37-4.35 (1H, m), 4.29-4.17 (3H, m), 4.06-4.02 (1H, m), 3.91-3.84 (2H, m), 3.76-3.69 (2H, m), 2.53-2.41 (2H, m), 2.20-2.11 (1H, m), 2.05 (1H, brs), 1.94-1.88 (2H, m), 1.29 (3H, t, J=7 Hz).
##STR00177##
Ethyl (2S,3S)-8-[N-(2,4-difluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 145 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as an amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 6.9 minutes
high polarity compound (second peak): 10.7 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.62-7.57 (1H, m), 6.93-6.86 (3H, m), 4.36 (1H, d, J=4 Hz), 4.29-4.18 (3H, m), 4.06-4.01 (1H, m), 3.91-3.84 (2H, m), 3.75-3.70 (2H, m), 2.52-2.42 (2H, m), 2.19-1.50 (4H, m), 1.29 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.62-7.57 (1H, m), 6.93-6.87 (3H, m), 4.36 (1H, dd, J=6 Hz, 3 Hz), 4.29-4.18 (3H, m), 4.13-4.09 (1H, m), 3.91 (1H, dd, J=12 Hz, 4 Hz), 3.84 (1H, dd, J=12 Hz, 4 Hz), 3.75-3.70 (2H, m), 2.51-2.40 (2H, m), 2.20-1.50 (4H, m), 1.29 (3H, t, J=7 Hz).
##STR00178##
Ethyl (2R,3R)-8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 146 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as an amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel Chemical
Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 6.8 minutes
high polarity compound (second peak): 8.8 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9.2 Hz, 5.2 Hz), 7.34 (1H, dd, J=7.6 Hz, 2.9 Hz), 7.11-7.06 (1H, m), 6.91 (1H, s), 4.44 (1H, dd, J=5.8 Hz, 2.0 Hz), 4.28-4.10 (4H, m), 3.93-3.70 (4H, m), 2.60-2.47 (2H, m), 2.24-2.14 (1H, m), 1.97-1.92 (1H, m), 1.27 (3H, t, J=7.0 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9.2 Hz, 5.3 Hz), 7.34 (1H, dd, J=7.6 Hz, 2.9 Hz), 7.11-7.06 (1H, m), 6.85 (1H, s), 4.44 (1H, d, J=5.0 Hz), 4.27-4.02 (4H, m), 3.92-3.84 (2H, m), 3.76-3.70 (2H, m), 2.61-2.48 (2H, m), 2.23-2.15 (1H, m), 1.92-1.88 (1H, m), 1.27 (3H, t, J=7.2 Hz).
##STR00179##
Ethyl (2S,3S)-8-[N-(2-bromo-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 147 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as an amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 6.7
minutes
high polarity compound (second peak):
13.2 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.33 (1H, dd, J=8 Hz, 3 Hz), 7.10-7.06 (1H, m), 6.84 (1H, s), 4.44 (1H, d, J=5 Hz), 4.24-3.70 (8H, m), 2.61-2.48 (2H, m), 2.24-1.87 (2H, m), 1.26 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9 Hz, 5 Hz), 7.33 (1H, dd, J=8 Hz, 3 Hz), 7.10-7.05 (1H, m), 6.91 (1H, s), 4.44 (1H, d, J=6 Hz), 4.27-3.69 (8H, m), 2.59-2.48 (2H, m), 2.23-1.91 (2H, m), 1.26 (3H, t, J=7 Hz).
##STR00180##
Ethyl (2R,3R)-8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 148 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a pale red amorphous substance and a white powder. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 5.02
minutes
high polarity compound (second peak):
5.24 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.98-6.93 (2H, m), 6.90 (1H, dt, J=8 Hz, 3 Hz), 6.67 (1H, s), 4.40 (1H, dd, J=6 Hz, 3 Hz), 4.29-4.19 (3H, m), 4.13-4.08 (1H, m), 3.92 (1H, dd, J=12 Hz, 4 Hz), 3.85 (1H, dd, 12 Hz, 4 Hz), 3.76-3.69 (2H, m), 2.78-2.62 (2H, m), 2.53-2.35 (2H, m), 2.19-1.80 (4H, m), 1.65-1.49 (2H, m), 1.44-1.34 (2H, m), 1.31 (3H, t, J=7 Hz), 0.95 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.95 (1H, dd, J=9 Hz, 3 Hz), 6.93-6.86 (2H, m), 6.62 (1H, s), 4.41 (1H, d, J=4 Hz), 4.28-4.17 (3H, m), 4.05-4.01 (1H, m), 3.91-3.83 (2H, m), 3.77-3.69 (2H, m), 2.77-2.62 (2H, m), 2.53-2.35 (2H, m), 2.18-1.76 (4H, m), 1.65-1.50 (2H, m), 1.44-1.35 (2H, m), 1.30 (3H, t, J=7 Hz), 0.95 (3H, t, J=7 Hz).
##STR00181##
Ethyl (2S,3S)-8-[N-(2-butyl-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 149 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white powder and a pale red amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 5.08
minutes
high polarity compound (second peak):
5.58 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47 (1H, dd, J=9 Hz, 5 Hz), 6.95 (1H, dd, J=9 Hz, 3 Hz), 6.93-6.86 (2H, m), 6.61 (1H, s), 4.41 (1H, d, J=4 Hz), 4.26-4.16 (3H, m), 4.05-3.99 (1H, m), 3.90-3.80 (2H, m), 3.78-3.68 (2H, m), 2.77-2.62 (2H, m), 2.53-2.39 (2H, m), 2.33-2.05 (2H, m), 1.96-1.86 (1H, m), 1.80-1.65 (1H, m), 1.63-1.52 (2H, m), 1.44-1.35 (2H, m), 1.29 (3H, t, J=7 Hz), 0.95 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.99-6.86 (3H, m), 6.70 (1H, s), 4.40 (1H, dd, J=6 Hz, 3 Hz), 4.29-4.17 (3H, m), 4.13-4.07 (1H, m), 3.90 (1H, dd, J=12 Hz, 4 Hz), 3.84 (1H, dd, 12 Hz, 4 Hz), 3.76-3.69 (2H, m), 2.77-2.62 (2H, m), 2.53-2.23 (3H, m), 2.20-2.00 (2H, m), 1.96-1.86 (1H, m), 1.63-1.52 (2H, m), 1.44-1.34 (2H, m), 1.30 (3H, t, J=7 Hz), 0.95 (3H, t, J=7 Hz).
##STR00182##
Ethyl (2R,3R)-8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 150 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a pale red amorphous substance and a white powder. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 4.83
minutes
high polarity compound (second peak):
5.01 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.92 (2H, m), 6.90 (1H, dt, J=8 Hz, 3 Hz), 6.66 (1H, s), 4.40 (1H, dd, J=6 Hz, 3 Hz), 4.28-4.18 (3H, m), 4.14-4.07 (1H, m), 3.92 (1H, dd, J=12 Hz, 4 Hz), 3.85 (1H, dd, 12 Hz, 4 Hz), 3.76-3.69 (2H, m), 2.76-2.61 (2H, m), 2.50-2.35 (2H, m), 2.19-2.08 (1H, m), 1.97-1.87 (1H, m), 1.81-1.49 (4H, m), 1.40-1.32 (4H, m), 1.30 (3H, t, J=7 Hz), 0.90 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.95 (1H, dd, J=9 Hz, 3 Hz), 6.93-6.86 (2H, m), 6.60 (1H, s), 4.41 (1H, d, J=5 Hz), 4.29-4.17 (3H, m), 4.07-4.01 (1H, m), 3.93-3.84 (2H, m), 3.76-3.69 (2H, m), 2.76-2.61 (2H, m), 2.54-2.36 (2H, m), 2.19-2.07 (1H, m), 2.06-1.70 (3H, m), 1.66-1.50 (2H, m), 1.40-1.32 (4H, m), 1.30 (3H, t, J=7 Hz), 0.90 (3H, t, J=7 Hz).
##STR00183##
Ethyl (2S,3S)-8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 151 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white powder and a pale red amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purity were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 4.90
minutes
high polarity compound (second peak):
6.18 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.85 (3H, m), 6.59 (1H, s), 4.40 (1H, d, J=5 Hz), 4.29-4.17 (3H, m), 4.06-4.00 (1H, m), 3.91-3.83 (2H, m), 3.76-3.69 (2H, m), 2.76-2.59 (2H, m), 2.53-2.36 (2H, m), 2.20-2.06 (1H, m), 1.94-1.85 (1H, m), 1.80-1.50 (4H, m), 1.41-1.22 (7H, m), 0.91 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.92 (2H, m), 6.89 (1H, dt, J=8 Hz, 3 Hz), 6.73 (1H, s), 4.40 (1H, dd, J=6 Hz, 3 Hz), 4.28-4.17 (3H, m), 4.12-4.05 (1H, m), 3.89 (1H, dd, J=12 Hz, 4 Hz), 3.82 (1H, dd, 12 Hz, 4 Hz), 3.76-3.69 (2H, m), 2.76-2.61 (2H, m), 2.51-2.35 (2H, m), 2.26-2.01 (2H, m), 1.97-1.68 (2H, m), 1.66-1.54 (2H, m), 1.41-1.31 (4H, m), 1.29 (3H, t, J=7 Hz), 0.90 (3H, t, J=7 Hz).
##STR00184##
Ethyl (2R,3R)-8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 152 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as an amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 9:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 25.2
minutes
high polarity compound (second peak):
29.3 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.87 (3H, m), 6.66 (1H, s), 4.41-4.37 (1H, m), 4.29-4.19 (3H, m), 4.13-4.09 (1H, m), 3.95-3.88 (1H, m), 3.87-3.81 (1H, m), 3.77-3.69 (2H, m), 2.77-2.62 (2H, m), 2.51-2.36 (2H, m), 2.19-2.09 (2H, m), 1.95-1.89 (2H, m), 1.63-1.52 (2H, m), 1.40-1.28 (9H, m), 0.91-0.86 (3H, m).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.86 (3H, m), 6.63 (1H, s), 4.42-4.39 (1H, m), 4.30-4.16 (3H, m), 4.06-4.01 (1H, m), 3.91-3.83 (2H, m), 3.77-3.69 (2H, m), 2.76-2.61 (2H, m), 2.53-2.37 (2H, m), 2.18-2.08 (2H, m), 2.03-1.98 (1H, m), 1.93-1.86 (1H, m), 1.63-1.52 (2H, m), 1.41-1.26 (9H, m), 0.91-0.86 (3H, m).
##STR00185##
Ethyl (2S,3S)-8-[N-(4-fluoro-2-hexylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 153 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purity two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as an amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 7.6
minutes
high polarity compound (second peak):
10.6 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.95 (1H, dd, J=9 Hz, 3 Hz), 6.92-6.87 (2H, m), 6.61 (1H, s), 4.40 (1H, d, J=4 Hz), 4.29-4.17 (3H, m), 4.06-4.02 (1H, m), 3.91-3.84 (2H, m), 3.76-3.70 (2H, m), 2.75-2.62 (2H, m), 2.52-2.46 (1H, m), 2.42 (1H, td, J=14 Hz, 3 Hz), 2.17-2.09 (1H, m), 2.05 (1H, dd, J=8 Hz, 5 Hz), 1.96-1.87 (2H, m), 1.64-1.53 (2H, m), 1.40-1.27 (9H, m), 0.91-0.87 (3H, m).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.93 (2H, m), 6.90 (1H, td, J=8 Hz, 3 Hz), 6.67 (1H, m), 4.39 (1H, dd, J=6 Hz, 4 Hz), 4.30-4.19 (3H, m), 4.13-4.09 (1H, m), 3.91 (1H, dt, J=12 Hz, 4 Hz), 3.84 (1H, dt, J=12 Hz, 4 Hz), 3.76-3.69 (2H, m), 2.76-2.63 (2H, m), 2.50-2.44 (1H, m), 2.40 (1H, td, J=13 Hz, 3 Hz), 2.18-2.10 (2H, m), 1.95-1.89 (2H, m), 1.63-1.53 (2H, m), 1.40-1.28 (9H, m), 0.91-0.87 (3H, m).
##STR00186##
Ethyl (2R,3R)-8-[N-(4-fluoro-2-heptylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 154 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify the two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 9:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 23.9
minutes
high polarity compound (second peak):
27.4 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=8 Hz, 5 Hz), 6.96-6.88 (3H, m), 6.67 (1H, s), 4.40-4.38 (1H, m), 4.27-3.69 (8H, m), 2.72-2.62 (2H, m), 2.49-1.89 (6H, m), 1.34-1.25 (11H, m), 0.88 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.47 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.87 (3H, m), 6.64 (1H, brs), 4.40 (1H, d, J=4 Hz), 4.29-3.71 (8H, m), 2.75-2.61 (2H, m), 2.51-2.37 (2H, m), 2.17-1.86 (4H, m), 1.42-1.22 (11H, m), 0.88 (3H, t, J=7 Hz).
##STR00187##
Ethyl (2S,3S)-8-[N-(4-fluoro-2-heptylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 155 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white powder and a white amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 4.8
minutes
high polarity compound (second peak): 6.3
minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.88 (3H, m), 6.64 (1H, s), 4.41 (1H, d, J=4 Hz), 4.27-3.72 (8H, m), 2.75-2.62 (2H, m), 2.51-2.38 (2H, m), 2.18-1.38 (4H, m), 1.38-1.28 (11H, m), 0.88 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.88 (3H, m), 6.69 (1H, s), 4.41-4.39 (1H, m), 4.29-3.71 (8H, m), 2.77-2.62 (2H, m), 2.49-1.90 (6H, m), 1.38-1.29 (11H, m), 0.89 (3H, t, J=7 Hz).
##STR00188##
Ethyl (2R,3R)-8-[N-(4-fluoro-2-octylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 156 was subjected to high performance liquid chromatography (column; CHIPALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 9:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 22.9
minutes
high polarity compound (second peak):
25.8 minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.96-6.88 (3H, m), 6.68 (1H, s), 6.68-4.40 (1H, m), 4.28-3.70 (8H, m), 4.28-3.70 (2H, m), 2.52-1.89 (6H, m), 1.36-1.19 (13H, m), 0.88 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.46 (1H, dd, J=9 Hz, 5 Hz), 6.95-6.87 (3H, m), 4.40 (1H, d, J=5 Hz), 4.28-3.71 (8H, m), 2.73-2.60 (2H, m), 2.50-1.87 (6H, m), 1.31-1.25 (13H, m), 0.89 (3H, t, J=7 Hz).
##STR00189##
Ethyl (2S,3S)-8-[N-(4-fluoro-2-octylphenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 157 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white powder and a colorless oil. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 4.7
minutes
high polarity compound (second peak): 6.1
minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.48 (1H, dd, J=9 Hz, 5 Hz), 6.97-6.88 (3H, m), 6.63 (1H, s), 4.41 (1H, d, J=5 Hz), 4.28-3.71 (8H, m), 2.75-2.62 (2H, m), 2.51-1.88 (6H, m), 1.38-1.27 (13H, m), 0.88 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=9 Hz, 6 Hz), 6.97-6.88 (3H, m), 6.97-6.88 (1H, m), 4.41-4.38 (1H, m), 4.31-3.71 (8H, m), 2.77-2.63 (2H, m), 2.50-1.90 (6H, m), 2.50-1.90 (13H, m), 0.88 (3H, t, J=7 Hz).
##STR00190##
Following the process described in Example (17a), 1,4-di-O-methyl-2,3-di-O-trimethylsilyl-D-threitol was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a colorless oil (yield: 89%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68-7.64 (1H, m), 7.16 (1H, dd, J=8.1 Hz, 3.0 Hz), 7.17-7.16 (3H, m), 4.39 (1H, d, J=3.5 Hz), 4.24-3.98 (4H, m), 3.43-3.42 (4H, m), 3.43 (1.5H, s), 3.42 (1.5H, s), 3.39 (1.5H, s), 3.38 (1.5H, s), 2.57-2.45 (2H, m), 2.57-2.45 (1H, m), 1.96-1.86 (1H, m), 1.27 (3H, dt, J=6.9 Hz, 2.1 Hz).
##STR00191##
Following the process described in Example (17a), 1,4-di-O-methyl-2,3-di-O-trimethylsilyl-L-threitol was used in place of 1,4-di-o-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a colorless oil (91% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68-7.64 (1H, m), 7.16 (1H, dd, J=7.8 and 2.4 Hz), 7.04-7.00 (2H, m), 6.89 (1H, s), 4.40-4.39 (1H, m), 4.23-3.97 (4H, m), 3.62-3.47 (4H, m), 3.43 (1.5H, s), 3.41 (1.5H, s), 3.39 (1.5H, s), 3.38 (1.5H, s), 2.58-2.45 (2H, m), 2.26-2.16 (1H, m), 1.96-1.86 (1H, m), 1.26 (3H, dt, J=7.0 and 3.5 Hz).
##STR00192##
Following the process described in Example (17a), 1,4-di-O-benzyl-2,3-di-o-trimethylsilyl-L-threitol was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a colorless oil (yield: 94%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.69-7.64 (1H, m), 7.37-7.26 (10H, m), 7.16 (1H, dd, J=7.8 Hz, 2.8 Hz), 7.04-6.90 (3H, m), 4.64-4.51 (4H, m), 4.40 (1H, t, J=4.5 Hz), 4.30-4.05 (4H, m), 3.68-3.57 (4H, m), 2.58-2.45 (2H, m), 2.25-2.17 (1H, m), 1.96-1.86 (1H, m), 1.21 (3H, dt, J=7.0 Hz, 3.5 Hz).
##STR00193##
Following the process described in Example (17a), 1,4-di-O-acetyl-2,3-di-O-trimethylsilyl-D-threitol obtained in Reference Example 24 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a white amorphous substance (50% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.67 (1H, dd, J=9.2 Hz, 5.3 Hz), 7.17 (1H, dd, J=7.9 Hz, 2.8 Hz), 7.05-7.00 (2H, m), 6.90-6.76 (1H, m), 4.41 (1H, d, J=4.7 Hz), 4.37-4.37 (8H, m), 2.60-2.46 (2H, m), 2.23-2.04 (8H, m), 1.26 (3H, t, J=7.0 Hz).
##STR00194##
218 mg (1.07 mmol) of N-(4-acetylamino-2R,3R-dihydroxybutyl)acetamide and 0.57 ml (3.20 mmol) of isopropoxytrimethylsilane were dissolved in 3 ml of nitromethane, and 13 μl (0.071 mmol) of trimethylsilyl trifluoromethanesulfonate and 300 mg (0.711 mmol) of ethyl 6-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-3,3-dimethoxy-1-cyclohexene-1-carboxylate obtained in Example (16a) were sequentially added thereto with stirring under ice-cooling, followed by stirring for 3 hours at the same temperature and then for 116 hours at room temperature. To the reaction solution was added saturated aqueous sodium hydrogencarbonate and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate methanol=9:1) to give 203 mg of the title compound as an amorphous substance (yield: 51%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68-7.63 (1H, m), 7.20-7.15 (1H, m), 7.08-7.00 (2H, m), 6.78-6.73 (1H, m), 6.46-6.38 (1H, m), 6.34-6.26 (1H, m), 4.42-4.39 (1H, m), 4.29-4.14 (2H, m), 3.96-3.85 (1.5H, m), 3.75-3.69 (0.5H, m), 3.61-3.42 (4H, m), 2.55-2.43 (2H, m), 2.21-2.01 (7H, m), 1.90-1.78 (1H, m), 1.31-1.25 (3H, m).
##STR00195##
Following the process described in Example 17 (alternative procedure), (1R,2R,3R,4R)-4-benzoyloxy-1-methyl-2,3-bis[(trimethylsilyl)oxy]pentyl benzoate obtained in Reference Example 25 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a white amorphous substance (yield: 33%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.66 (1H, dd, J=9.0 and 5.0 Hz), 7.17 (1H, dd, J=7.8 and 2.7 Hz), 7.09 (1H, d, J=9.0 Hz), 7.05-7.00 (1H, m), 6.80 (0.5H, s), 6.76 (0.5H, s), 4.39 (1H, d, J=5.4 Hz), 4.27-4.09 (2H, m), 3.88-3.56 (4H, m), 2.50-2.42 (2H, m), 2.19-2.11 (1H, m), 1.85-1.79 (1H, m), 1.33 (3H, t, J=5.3 Hz), 1.27 (6H, t, J=7.0 Hz).
##STR00196##
Following the process described in Example 17 (alternative procedure), (1R,2R,3R,4R)-4-benzoyloxy-1-ethyl-2,3-bis[(trimethylsilyl)oxy]hexyl benzoate obtained in Reference Example 26 was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a white amorphous substance (yield: 21%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.68 (1H, dd, J=9.2 Hz, 5.2 Hz), 7.18 (1H, dd, J=7.4 Hz, 2.4 Hz), 7.06-7.01 (2H, m), 6.81 (0.5H, s), 6.78 (0.5H, s), 4.40 (1H, d, J=5.1 Hz), 4.29-4.12 (2H, m), 3.88-3.55 (4H, m), 3.03 (1H, brs), 2.92 (1H, brs), 2.51-2.41 (2H, m), 2.21-2.13 (2H, m), 1.90-1.73 (1H, m), 1.55-1.43 (3H, m), 1.29 (3H, t, J=7.2 Hz), 1.05-0.97 (6H, m).
##STR00197##
Following the process described in Example (17a), (3R,4R,5R)-3,4-bis[(trimethylsilyl)oxy]-5-[(trimethylsilyl)oxy]methyldihydrofuran-2-one was used in place of 1,4-di-O-benzoyl-2,3-di-O-trimethylsilyl-D-threitol to give the title compound as a white amorphous substance (yield: 25%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.69-7.64 (1H, m), 7.20-7.16 (1H, m), 7.06-6.96 (2H, m), 6.82-6.68 (1H, m), 5.04-4.62 (3H, m), 4.44-4.40 (1H, m), 4.26-4.14 (2H, m), 4.05-3.98 (1H, m), 3.90-3.81 (1H, m), 2.74-2.46 (2H, m), 2.24-2.12 (1H, m), 1.97-1.83 (2H, m), 1.30-1.26 (3H, m).
##STR00198##
Ethyl (2R,3R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis((1R)-1,2-dihydroxyethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 23 was subjected to high performance liquid chromatography (column; CHIRALPAK AD-H, size; inner diameter 2 cm, length 25 cm, solvent; hexane:2-propanol) to separate and purify two optical isomers, and low polarity compound (first peak) and high polarity compound (second peak) were respectively obtained as a white amorphous substance. According to the result of HPLC analysis of the two optical isomers obtained under the conditions below, their optical purities were respectively >99% ee.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 7.3
minutes
high polarity compound (second peak): 9.9
minutes
(Low Polarity Compound, First Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.65 (1H, dd, J=9 Hz, 5 Hz), 7.21 (1H, bs), 7.17 (1H, dd, J=8 Hz, 3 Hz), 7.06-6.99 (1H, m), 6.80 (1H, s), 4.38 (1H, d, J=5 Hz), 4.27-4.12 (4H, m), 4.08 (2H, d, J=7 Hz), 3.95-3.88 (1H, m), 3.87-3.64 (5H, m), 2.98-2.68 (2H, m), 2.54-2.42 (2H, m), 2.22-2.08 (1H, m), 1.91-1.82 (1H, m), 1.25 (3H, t, J=7 Hz).
(High Polarity Compound, Second Peak)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.63 (1H, dd, J=9 Hz, 5 Hz), 7.15 (1H, bs), 7.12 (1H, dd, J=8 Hz, 3 Hz), 7.05-6.97 (1H, m), 6.76 (1H, s), 4.37 (1H, d, J=6 Hz), 4.27-4.01 (5H, m), 3.97-3.86 (2H, m), 3.85-3.45 (5H, m), 2.77-2.57 (2H, m), 2.52-2.41 (2H, m), 2.21-2.08 (1H, m), 1.89-1.80 (1H, m), 1.26 (3H, t, J=7 Hz).
##STR00199##
235 mg (0.49 mmol) of ethyl (2R,3R)-8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-2,3-bis(hydroxymethyl)-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 17 was dissolved in 1.5 ml of acetone, and 84 mg (0.59 mmol) of methyl iodide and 138 mg (1.00 mmol) of potassium carbonate were added sequentially, followed by stirring for 3 hours at 50° C. After the reaction solution was filtered, the filtrate was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (solvent; hexane ethyl acetate=1:3) to give 175 mg of the title compound as a white amorphous substance (yield: 73%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.57 (1H, brs), 7.22 (1H, dd, J=8 Hz, 3 Hz), 7.05-7.00 (1H, m), 6.87 (0.5H, s), 6.79 (0.5H, s), 4.58 (1H, brs), 4.28-3.73 (8H, m), 3.25 (3H, s), 2.60-1.80 (6H, m), 1.26 (3H, t, J=7 Hz).
##STR00200##
Following the process described in Example (id), 4-fluoro-2-propylphenylamine obtained in Reference Example 27 was used in place of 2-chloro-4-fluoroaniline to give the title compound as an oil (yield: 84%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.09-8.07 (4H, m), 7.59-7.55 (2H, m), 7.47-7.43 (4H, m), 7.47-7.43 (2H, m), 3.96 (2H, s), 2.00-1.79 (4H, m), 1.02 (6H, t, J=7 Hz), 0.07 (18H, s).
##STR00201##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-propylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 188 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a white amorphous substance (38% yield). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Da cel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 9.6
minutes
high polarity compound (second peak):
14.1 minutes
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.51-7.47 (1H, m), 6.97-6.88 (3H, m), 6.70 (0.5H, s), 6.64 (0.5H, s), 4.42-4.39 (1H, m), 4.28-3.72 (8H, m), 2.75-2.61 (2H, m), 2.52-2.37 (2H, m), 2.19-1.87 (4H, m), 1.68-1.57 (2H, m), 1.32-1.28 (3H, m), 0.99 (3H, t, J=8 Hz).
##STR00202##
Following the process described in Examples 7, (16a) and 23, ethyl 8-[N-(4-fluoro-2-pentylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 86 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as a white powder (yield: 33%). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 7:3
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 5.29
minutes
high polarity compound (second peak):
5.82 minutes
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49-7.44 (1H, m), 6.97-6.86 (2H, m), 6.84 (0.5H, m), 6.82 (0.5H, m), 6.73 (0.5H, s), 6.69 (0.5H, s), 4.41-4.36 (1H, m), 4.27-4.17 (2H, m), 4.12-4.01 (1.5H, m), 3.97-3.88 (1.5H, m), 3.88-3.67 (5H, m), 2.77-2.60 (2H, m), 2.50-2.30 (2H, m), 2.20-1.40 (8H, m), 1.39-1.25 (7H, m), 0.93-0.86 (3H, m).
##STR00203##
Following the process described in Examples 7, (16a) and 18 (alternative procedure), ethyl 8-[N-(4-fluoro-2-methylphenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate obtained in Example 79 was used in place of ethyl 8-[N-(2-chloro-4-fluorophenyl)sulfamoyl]-1,4-dioxaspiro[4.5]dec-6-ene-7-carboxylate to give the title compound as an amorphous substance (yield: 49%). This compound was separable into two optical isomers in accordance with the following HPLC conditions.
HPLC conditions
Column
CHIRALPAK AD-H (produced by Daicel
Chemical Industries, Ltd.
inner diameter 0.46 cm, length 25 cm)
Mobile phase
hexane:2-propanol = 4:1
Flow rate
1.0 ml/min
Temperature
40° C.
Detection
254 nm (UV)
Retention time
low polarity compound (first peak): 13.5
minutes
high polarity compound (second peak):
19.6 minutes
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.49 (1H, dd, J=8.8 Hz, 5.3 Hz), 6.96-6.88 (3H, m), 6.70 (0.5H, brs), 6.64 (0.5H, brs), 4.40-4.37 (1H, m), 4.28-3.70 (8H, m), 2.51-2.32 (5H, m), 2.21-1.87 (2H, m), 1.31-1.27 (3H, m).
300 mg (0.90 mmol) of 1,4-di-O-benzoyl-meso-erythritol (compound described in J. Am. Chem. Soc., 82, 2585 (1960)), 0.28 ml (1.98 mmol) of triethylamine and 11 mg (0.09 mmol) of 4-dimethylaminopyridine were dissolved in 6 ml of dichloromethane, and 0.24 ml (1.89 mmol) of trimethylsilyl chloride was added thereto with stirring under ice-cooling, followed by stirring for 2 hours at the same temperature. To the reaction solution was added saturated aqueous sodium hydrogencarbonate and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; ethyl acetate alone) to give 418 mg of the title compound as a white powder (yield: 98%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.04 (4H, d, J=7 Hz), 7.55 (2H, t, J=7 Hz), 7.43 (4H, t, J=7 Hz), 4.53 (2H, dd, J=12 Hz, J=3 Hz), 4.36 (2H, dd, J=12 Hz, 5 Hz), 4.13-4.08 (2H, m) 0.13 (18H, s)
Following the process described in Reference Example 1, D-arabitol was used in place of 1,4-di-o-benzoyl-meso-erythritol to give the title compound as a colorless oil (yield: 26%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
3.84-3.80 (1H, m), 3.76-3.68 (3H, m), 3.63-3.54 (2H, m), 3.49 (1H, dd, J=10 Hz, J=7 Hz), 0.14-0.09 (45H, m).
Following the process described in Reference Example 1, 1,6-di-O-benzoyl-D-mannitol was used in place of 1,4-di-O-benzoyl-meso-erythritol to give the title compound as a pale brown oil (yield: 98%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.05 (4H, d, J=7 Hz), 7.55 (2H, t, J=7 Hz), 7.43 (4H, t, J=7 Hz), 4.59 (2H, dd, J=12 Hz, 2 Hz), 4.38-4.31 (2H, m), 4.24-4.20 (2H, m), 3.83 (2H, br.s), 0.17 (18H, s), 0.11 (18H, s).
1.00 g (5.55 mmol) of 2-phenyl[1.3]dioxan-5-ol, 1.16 ml (8.32 mmol) of triethylamine and 68 mg (0.56 mmol) of 4-dimethylaminopyridine were dissolved in 20 ml of dichloromethane, and 1.28 g (6.10 mmol) of 1-adamantanecarbonyl chloride was added thereto with stirring under ice-cooling, followed by stirring for 30 minutes at the same temperature, and then further for 15 hours at room temperature. Dichloromethane was distilled off under reduced pressure, and to the residue was added aqueous sodium hydrogencarbonate and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=9:1) to give 1.52 g of the title compound as a pale yellow powder (yield: 80%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.52-7.48 (2H, m), 7.42-7.33 (3H, m), 5.54 (1H, s), 4.68-4.66 (1H, m), 4.26-4.22 (2H, m), 4.18-4.13 (2H, m), 2.07-2.01 (3H, m), 2.01-1.97 (6H, m), 1.77-1.69 (6H, m).
400 mg (1.17 mmol) of 2-phenyl[1.3]dioxan-5-yl adamantane-1-carboxylate obtained in (4a) was dissolved in 8 ml of ethyl acetate and 400 mg of 20% palladium hydroxide-carbon (water content: 50%) was added thereto, followed by stirring for 4 hours under hydrogen atmosphere at room temperature. After the catalyst was filtered, the filtrate was concentrated under reduced pressure to give 294 mg of the title compound as a white powder (yield: 99%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.90-4.85 (1H, m), 3.84-3.76 (4H, m), 2.16-2.00 (5H, m), 1.94-1.87 (6H, m), 1.78-1.67 (6H, m).
Following the process described in Reference Example 1, 2-hydroxy-1-hydroxymethylethyl adamantane-1-carboxylate obtained in (4b) was used in place of 1,4-di-O-benzoyl-meso-erythritol to give the title compound as a colorless oil (yield: 70%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.85-4.79 (1H, m), 3.72-3.61 (4H, m), 2.04-1.97 (3H, m), 1.92-1.83 (6H, m), 1.76-1.65 (6H, m), 0.11 (18H, s).
Following the process described in Reference Example 1, diethyl 2,2-bis(hydroxymethyl)malonate was used in place of 1,4-di-O-benzoyl-meso-erythritol to give the title compound as a colorless oil (yield: 75%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.17 (4H, q, J=7 Hz), 4.04 (4H, s), 1.23 (6H, t, J=7 Hz), 0.07 (18H, s).
2.0 g (14.47 mmol) of 2-pentylfuran was dissolved in 60 ml of dichloromethane, and 3.84 g (14.47 mmol) of 65% m-chloroperbenzoic acid was added dropwise thereto with stirring under ice-cooling, followed by stirring for 1 hour at the same temperature. To the reaction solution was added saturated aqueous sodium carbonate and the mixture was extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and was then concentrated under reduced pressure to give 1.62 g of the title compound as a yellow oil (yield: 73%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
10.23 (1H, d, J=7 Hz), 6.95 (1H, d, J=12 Hz), 6.18 (1H, dd, J=12 Hz, 7 Hz), 2.26 (2H, t, J=7 Hz), 1.73-1.61 (2H, m), 1.40-1.26 (4H, m), 0.91 (3H, t, J=6 Hz).
1.62 g (10.5 mmol) of (2E)-4-oxo-2-nonenal obtained in (6a) was dissolved in 30 ml of ethyl acetate, and 160 mg of 10% palladium-carbon (water content: 50%) was added thereto, followed by restirring for 2 hours under hydrogen atmosphere at room temperature. After the catalyst was filtered, the filtrate was concentrated under reduced pressure to give 1.50 g of the title compound as a pale yellow oil (91% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
9.81 (1H, s), 2.81-2.67 (4H, m), 2.47 (2H, t, J=7 HZ), 1.67-1.53 (2H, m), 1.38-1.21 (4H, m), 0.89 (3H, t, J=7 Hz).
1.50 g (9.60 mmol) of 4-oxononanal obtained in (6b) was dissolved in 45 ml of ethanol-acetic acid (2:1) solution mixture, and 1.60 g (9.60 mmol) of benzyl hydrazinecarboxylate was added thereto, followed by stirring for 1 hour at 80° C. The reaction solution was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 2.12 g of the title compound as a yellow oil (77% yield).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.36 (5H, bs), 7.21 (1H, ds), 6.63-6.59 (1H, m), 6.07 (1H, t, J=4 Hz), 5.89-5.84 (1H, m), 5.22 (2H, ds), 2.46-2.36 (2H, m), 1.63-1.49 (2H, m), 1.37-1.22 (4H, m), 0.88 (3H, t, J=7 Hz).
1.0 g (3.49 mmol) of benzyl 2-pentyl-1H-pyrrol-1-ylcarbamate obtained in (6c) was dissolved in 20 ml of ethanol, and 100 mg of 10% palladium-carbon (water content: 50%) was added thereto, followed by stirring for 2 hours under hydrogen atmosphere at room temperature. After the catalyst was filtered, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=2:1) to give 430 mg of the title compound as a yellow oil (yield: 81%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.68 (1H, m), 5.97 (1H, t, J=3 Hz), 5.82-5.77 (1H, m), 4.52 (2H, s), 2.58 (2H, t, J=8 Hz), 1.69-1.57 (2H, m), 1.44-1.31 (4H, m), 0.91 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 6, 2-hexylfuran was used as the starting material in place of 2-pentylfuran to give the title compound as a yellow oil (yield: 29%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.67-6.63 (1H, m), 5.99-5.94 (1H, m), 5.81-5.77 (1H, m), 4.52 (2H, br.s), 2.62-2.55 (2H, m), 1.67-1.56 (2H, m), 1.44-1.21 (6H, m), 0.89 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 6, 2-heptylfuran was used as the starting material in place of 2-pentylfuran to give the title compound as a pale yellow solid (yield: 59%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.67-6.63 (1H, m), 5.99-5.94 (1H, m), 5.81-5.77 (1H, m), 4.52 (2H, br.s), 2.62-2.55 (2H, m), 1.67-1.53 (2H, m), 1.44-1.21 (8H, m), 0.89 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 6, 2-octylfuran was used as the starting material in place of 2-pentylfuran to give the title compound as a yellow oil (yield: 11%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.65-6.61 (1H, m), 5.97-5.93 (1H, m), 5.78-5.75 (1H, m), 4.51 (2H, br.s), 2.60-2.55 (2H, m), 1.66-1.54 (2H, m), 1.42-1.21 (10H, m), 0.88 (3H, t, J=7 Hz).
230 mg (1.79 mmol) of 1-cyclopropyl-4-hydroxy-1-butanone was dissolved in 7 ml of dichloromethane, and 580 mg (2.69 mmol) of pyridinium chlorochromate was added thereto, followed by stirring for 1 hour at room temperature. To the reaction solution was added diethyl ether, the mixture was filtered using Celite, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; diethyl ether alone) to give 176 mg of the title compound as a pale yellow oil (yield: 78%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
9.78 (1H, s), 2.91 (2H, t, J=7 Hz), 2.78-2.71 (2H, m), 2.01-1.93 (1H, m), 1.08-1.01 (2H, m), 0.96-0.88 (2H, m).
Following the procedures described in Reference Examples (6c) and (6d), 4-cyclopropyl-4-oxobutanal obtained in (10a) was used in place of 4-oxononanal to give the title compound as a pale yellow oil (yield: 45%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.70-6.64 (1H, m), 5.94-5.88 (1H, m), 5.71-5.64 (1H, m), 4.69 (2H, br.s), 1.83-1.72 (1H, m), 0.91-0.83 (2H, m), 0.64-0.57 (2H, m).
3.0 g (7.0 mmol) of hexyltriphenylphosphonium bromide was suspended in 30 ml of tetrahydrofuran, and 4.5 ml (7.0 mmol) of n-butyl lithium/hexane solution (1.56 M) was added dropwise thereto at −10° C. After the reaction solution was stirred for 10 minutes at the same temperature, 846 mg (5.0 mmol) of 4-fluoro-2-nitrobenzaldehyde was added, and the reaction solution was further stirred for 1 hour. To the reaction solution was added 1N aqueous potassium hydrogensulfate and the mixture was extracted with ethyl acetate. The organic layer was washed sequentially with saturated aqueous sodium hydrogencarbonate and water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=19:1) to give 917 mg of the title compound as a pale yellow oil (yield: 77%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.09 (1.7H, dd, J=9 Hz, 5 Hz), 7.97 (1H, dd, J=9 Hz, 5 Hz), 7.26-6.99 (5.4H, m), 6.89 (1H, d, J=16 Hz), 6.69 (1.7H, d, J=11 Hz), 6.26 (1H, dt, J=16 Hz, 7 Hz), 5.87 (1.7H, dt, J=12 Hz, 8 Hz), 2.28 (2H, q, J=7 Hz), 2.10 (3.4H, q, J=7 Hz), 1.52-1.23 (16.2H, m), 0.91 (3H, m), 0.86 (5.1H, m).
910 mg (3.8 mmol) of 4-fluoro-2-(hept-1-enyl)-1-nitrobenzene obtained in (11a) was dissolved in 5 ml of ethanol, and 100 mg of 10% palladium-carbon (water content: 50%) was added thereto, followed by stirring for 2 hours under hydrogen atmosphere at room temperature. After the catalyst was filtered, the filtrate was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=9:1) to give 730 mg of the title compound as a pale yellow oil (yield: 91%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.80-6.71 (2H, m), 6.61 (1H, dd, J=9 Hz, 5 Hz), 3.47 (2H, brs), 2.45 (2H, t, J=7 Hz), 1.64-1.58 (2H, m), 1.42-1.24 (8H, m), 0.89 (3H, t, J=6 Hz).
Following the procedure described in Reference Example 11, propyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a brown oil (yield: 78%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.80-6.69 (2H, m), 6.60 (1H, dd, J=9 Hz, 5 Hz), 3.51 (2H, bs), 2.46 (2H, t, J=8 Hz), 1.63-1.56 (2H, m), 1.45-1.37 (2H, m), 0.96 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 11, butyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a yellow oil (yield: 78%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.80-6.69 (2H, m), 6.60 (1H, dd, J=9 Hz, 5 Hz), 3.50 (2H, bs), 2.45 (2H, t, J=8 Hz), 1.64-1.58 (2H, m), 1.45-1.36 (4H, m), 0.91 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 11, pentyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a pale brown oil (yield: 63%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.81-6.71 (2H, m), 6.66 (1H, dd, J=9 Hz, 5 Hz), 4.19 (2H, brs), 2.48 (2H, t, J=8 Hz), 1.65-1.57 (2H, m), 1.43-1.25 (6H, m), 0.92-0.85 (3H, m).
Following the procedure described in Reference Example 11, heptyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a pale yellow oil (yield: 65%)
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.80-6.71 (2H, m), 6.61 (1H, dd, J=9 Hz, 5 Hz), 2.45 (2H, t, J=7 Hz), 1.64-1.56 (2H, m), 1.38-1.22 (10H, m), 0.88 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 11, octyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a pale brown oil (yield: 97%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
6.77 (1H, dd, J=10 Hz, 3 Hz), 6.72 (1H, td, J=8 Hz, 3 Hz), 6.59 (1H, dd, J=9 Hz, 5 Hz), 3.46 (2H, brs), 2.45 (2H, t, J=8 Hz), 1.64-1.56 (2H, m), 1.44-1.21 (12H, m), 0.88 (3H, t, J=7 Hz).
Following the procedure described in Reference Example 11, nonyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a pale brown oil (yield: 67%).
1H-NMR spectrum (500 MHz, CDCl3) δ ppm:
6.77 (1H, dd, J=10 Hz, 3 Hz), 6.73 (1H, dd, J=8 Hz, 3 Hz), 6.60 (1H, dd, J=9 Hz, 5 Hz), 3.47 (2H, brs), 2.45 (2H, t, J=8 Hz), 1.64-1.56 (2H, m), 1.43-1.21 (14H, m), 0.88 (3H, t, J=7 Hz).
17.48 g (52.9 mmol) of 1,4-di-C-benzoyl-D-threitol and 10.8 g (159 mmol) of imidazol were dissolved in 250 ml of dichloromethane, and 12.6 g (116 mmol) of chlorotrimethylsilane was added thereto with stirring under ice-cooling, followed by stirring for 1 hour at room temperature. The reaction solution was directly subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=20:1-5:1) to give 24.59 g of f the title compound as a white powder (yield: 98%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.04 (4H, dd, J=8 Hz, J=1 Hz), 7.57-7.52 (2H, m), 7.46-7.40 (4H, m), 4.50 (2H, dd, J=11 Hz, J=4 Hz), 4.48-4.33 (2H, m), 4.13-4.08 (2H, m), 0.14 (18H, s).
Following the process described in Reference Example 18, 1,4-di-O-benzoyl-L-threitol was used in place of 1,4-di-o-benzoyl-D-threitol to give the title compound as a white powder (yield: 98%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.04 (4H, dd, J=8 Hz, J=1 Hz), 7.57-7.52 (2H, m), 7.46-7.40 (4H, m), 4.50 (2H, dd, J=11 Hz, J=4 Hz), 4.48-4.33 (2H, m), 4.13-4.08 (2H, m), 0.14 (18H, s)
Following the process described in Reference Example 18, methyl (S)-3,4-dihydroxybutyrate was used in place of 1,4-di-O-benzoyl-D-threitol to give the title compound as an oil (yield: 62%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.18-4.12 (1H, m), 3.67 (3H, s), 3.52 (1H, dd, J=10 Hz, 6 Hz), 3.40 (1H, dd, J=10 Hz, 6 Hz), 2.59 (1H, dd, J=15 Hz, 5 Hz), 2.37 (1H, dd, J=15 Hz, 7 Hz), 0.10 (18H, s).
Following the process described in Reference Example 1, 1,4-anhydroerythritol was used in place of 1,4-di-o-benzoyl-meso-erythritol to give the title compound as a colorless oil (yield: 21%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.15-4.10 (2H, m), 3.92-3.85 (2H, m), 3.68-3.62 (2H, m), 0.14 (18H, s).
590 mg (5.0 mmol) of dimethyloxalate was dissolved in 20 ml of tetrahydrofuran, and 22 ml (22 mmol) of 1.0 M ethyl magnesium bromide/tetrahydrofuran solution was added thereto with stirring under ice-cooling, followed by stirring for 2 hours at the same temperature. The reaction solution was made acidic by addition of 1N hydrochloric acid and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=3:1) to give 276 mg of the title compound as an oil (yield: 38%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
3.45-3.41 (1H, m), 1.87 (1H, d, J=6 Hz), 1.75 (1H, s), 1.70-1.31 (6H, m), 1.04 (3H, t, J=7 Hz), 0.89 (3H, t, J=8 Hz), 0.89 (3H, t, J=8 Hz).
270 mg (1.85 mmol) of 3-ethylhexane-3,4-diol obtained in (22a) was dissolved in 5 ml of pyridine, and 597 mg (3.7 mmol) of 1,1,1,3,3,3-hexamethylsilazane and 1.20 g (11 mmol) of chlorotrimethylsilane were added sequentially, followed by stirring for 2 hours at the same temperature and further overnight at room temperature. To the reaction solution was added water and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=9:1) to give 469 mg of the title compound as an oil (yield: 88%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
3.38 (1H, dd, J=9.0 Hz, 3.0 Hz), 1.68-1.33 (6H, m), 0.90 (3H, t, J=6.0 Hz), 0.92-0.90 (6H, m), 0.11-0.08 (18H, m).
Following the process described in Reference Example 18, (R)-1,1,2-triphenyl-1,2-ethanediol was used in place of 1,4-di-O-benzoyl-D-threitol to give the title compound as a powder (yield: 99%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
7.28-7.18 (15H, m), 5.51 (1H, s), −0.05 (9H, s), −0.16 (9H, s).
Following the process described in Reference Example 18, 1,4-di-O-acetyl-D-threitol was used in place of 1,4-di-O-benzoyl-D-threitol to give the title compound as an oil (yield: 96%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
4.20 (2H, dd, J=11 Hz, 4 Hz), 4.01 (2H, dd, J=11 Hz, 7 Hz), 3.88-3.84 (2H, m), 2.06 (6H, s), 0.13 (18H, s).
Following the process described in Reference Example 18, (1R,2S,3S,4R)-4-benzoyloxy-2,3-dihydroxy-1-methylpentyl benzoate was used in place of 1,4-di-O-benzoyl-D-threitol to give the title compound as an oil (yield: 86%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.06-8.04 (4H, m), 7.57-7.54 (2H, m), 7.46-7.42 (4H, m), 5.31-5.25 (2H, m), 3.98-3.97 (2H, m), 1.41 (6H, d, J=6 Hz), 0.12 (18H, s).
Following the process described in Reference Example 18, (1R,2S,3S,4R)-4-benzoyloxy-1-ethyl-2,3-dihydroxyhexyl benzoate was used in place of 1,4-di-O-benzoyl-D-threitol to give the title compound as an oil (yield: 82%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
8.09-8.07 (4H, m), 7.59-7.55 (2H, m), 7.47-7.43 (4H, m), 7.47-7.43 (2H, m), 3.96 (2H, s), 2.00-1.79 (4H, m), 1.02 (6H, t, J=7 Hz), 0.07 (18H, s).
Following the process described in Reference Example 11, ethyltriphenylphosphonium bromide was used in place of hexyltriphenylphosphonium bromide to give the title compound as a pale yellow oil (yield: 17%).
1H-NMR spectrum (400 MHz, CDCl3) δ ppm:
6.80-6.59 (3H, m), 3.48 (2H, brs), 2.45 (2H, t, J=7 Hz), 1.70-1.58 (2H, m), 1.01 (3H, t, J=8 Hz).
The suppression rate of the compound according to the present invention against TNF-α production when human monocyte cell line U937 was stimulated by endotoxin, was measured. Specifically, to RPMI1640 medium containing 10% (volume %) of heat-inactivated new born calf serum, was added 12-O-tetradecanoylphorbol 13-acetate so that its final concentration became 30 ng/ml. U937 cells were suspended with the medium and plated to a 96 well culture plate (Sumilon) so that number of cells/volume was 2×104/0.1 ml, and were then cultured for 3 days at 37° C. in a carbon dioxide incubator with 5% CO2 and 100% humidity. After completion of incubation, the culture supernatant was removed. The compound according to the present invention was added to each of the wells in various concentrations, and lipopolysaccharide (LPS) (E. coli 0111:B4, Sigma) was also added so that its final concentration was 30 ng/ml. After incubating the culture plate in the carbon dioxide incubator again for 4.5 hours, the culture supernatant was collected. By using a 384 half well black plate (Greiner) and HTRF quantitative kit of CIS Bio International, the concentration of TNF-α in the culture supernatant was measured as time-resolved fluorescence with Discovery (Packard). From the measured value in the absence of LPS (X), measured value in the absence of the compound according to the present invention (Y) and measured value in the presence of the compound according to the present invention (Z), the suppression rate of TNF-α production was obtained by the following calculation formula [I].
Suppression rate of TNF-α production (%)={1−(Z−X)/(Y−X)}×100 [I]
In the present test, the compound according to the present invention showed an excellent suppression effect against endotoxin stimulated TNF-α production in cells.
The suppression effect of the compound according to the present invention against elevated TNF-α concentration in blood was evaluated. The test for TNF-α concentration elevation in blood was conducted in accordance with the process of Parant et al, which is described in Journal of Leukocyte Biology, Vol. 47, p. 164 (1990).
In the test, 3 to 4 male Sprague Dawley rats (8-9 weeks old) were used for each group.
4 hours before the administration of LPS, muramyl dipeptide dissolved in a physiological saline solution (1 mg/ml) was administered to the tail vein at a rate of 1 ml/kg. 0.5 hours before the administration of LPS, the rats were anaesthetized with pentobarbital (40 mg/kg), and the compound according to the present invention dissolved in 5% dimethyl acetamide/95% polyethylene glycol 400 solution was administered to the right femoral vein at a rate of 1 ml/kg. The control group was administered with 5% dimethyl acetamide/95% polyethylene glycol 400 solution at a rate of 1 ml/kg. LPS dissolved in a physiological saline solution (3 μg/ml) was administered to the left femoral vein at a rate of 1 ml/kg. 2 hours after the administration of LPS, blood was collected using 3.8% (w/v) sodium citrate solution as an anticoagulant, and blood plasma was separated by centrifuge (10,000 g, 5 minutes, 4° C.). TNF-α concentration in the blood plasma was measured using a TNF-α quantitative kit (Bio Source International, Inc.). From the TNF-α concentration in the blood of control group (X) and the TNF-α concentration in the blood of the group administered with the compound according to the present invention (Y), the TNF-α elevation suppression rate was calculated using the following calculation formula [II].
TNF-α elevation suppression rate (%)={1−Y/X}×100 [II]
In the present test, the compound according to the present invention showed excellent suppression effects against elevated TNF-α concentration in blood.
Kimura, Tomio, Ando, Osamu, Ohkawa, Nobuyuki, Nagasaki, Takayoshi, Sugidachi, Atsuhiro
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