A tetrazoleacetic acid derivative represented by the following general formula (I): ##STR1## [in Formula (I), wherein R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] except for [5-(2-thienyl)tetrazol-1-yl] acetic acid, [5-(2-furyl)tetrazol-1-yl) acetic acid, (5-(5-bromo-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylthio-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylsulfonyl-2-furyl)tetrazol-1-yl)acetic acid and ethyl esters thereof, or a salt thereof shows excellent aldose reductase inhibitory activity, has low toxicity to organisms and is quite effective as an essential component of a preventative medicine and/or remedy for diabetic complications.
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7. An aldose reductase inhibitor comprising a tetrazoleacetic acid derivative represented by the following general formula (II): ##STR9## [Formula (II) wherein, R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, and alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl gorup or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.
13. A method for alleviating or reducing diabetic complications wherein an effective amount of a tetrazoleacetic acid derivative represented by the following general formula (II): ##STR10## [in Formula (II) wherein, R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] or a pharmaceutically acceptable salt thereof is used administered.
1. A tetrazoleacetic acid derivative represented by the following general formula (I): ##STR8## [Formula (I) wherein, R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] except for [(5-(2-(thienyl)tetrazol-1-yl)] acetic acid, [(5-(2-(furyl)tetrazol-1-yl)] acetic acid, (5-(5-bromo-2-furyl)tetrazol-1-acetic acid, (5-(5-phenylthio-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylsulfonyl-2-furyl)tetrazol-1-yl)acetic acid and ethyl esters thereof, or a pharmaceutically acceptable salt thereof.
2. The tetrazoleacetic acid derivative of
3. The tetrazoleacetic acid derivative of
4. The tetrazoleactic acid derivative of
5. The tetrazoleacetic acid derivative of
6. The tetrazoleacetic acid derivative of
8. The aldose reductase inhibitor of
9. The aldose reductase inhibitor of
10. The aldose reductase inhibitor of
11. The aldose reductase inhibitor of
12. The aldose reductase inhibitor of
14. The method of
15. The method of
16. The method of
17. The method of
18. The method of
19. The method of
20. The method of calim 13 wherein the compound is administered in the form of tablets, powder, fine particles, granules, capsules, pills, liquid preparations, solutions or suspensions for injection or eye drops.
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1. Field of the Invention
The present invention relates to a compound having an aldose reductase inhibitory activity and more specifically to a tetrazoleacetic acid derivative and an aldose reductase inhibitor which comprises the tetrazoleacetic acid derivative as an effective component and which is effective as a preventive medicine and/or remedy for diabetic complications as well as a method for alleviating or reducing diabetic complications.
2. Prior Art
It has been known that aldose reductase inhibitors are effective for prevention and/or treatment of diabetic copmplications. This is detailed in the article of Dr. Tsuyoshi TANIMOTO [Division of Biological Chemistry and Reference Standards, National Institute of Hygienic Sciences] (see Farumashia, 1988,24 No. 5, pp. 459-463). This article discloses the chemical structures and 50% inhibitory concentrations (IC50) of representative aldose reductase inhibitors such as Alrestatin, Tolrestat, 4-Isopropyl-BFOC, Sorbinil, M-79175, Alconil, ADN-138, Epalrestat, CT-112 and Statil.
The inventors of this invention already conducted screening of novel aldose reductase inhibitors, found that compounds represented by the following general formula (III): ##STR2## [in Formula (III), R1 represents a hydrogen atom or a group: --A--COOR5 (wherein A represents an alkylene group having 1-4 carbon atoms and R5 represents a hydrogen atom or a lower alkyl group) and R2, R3 and R4 may be the same or different and each represents a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, a phenyl group, a phenoxy group, a nitro group, a residue represented by the formula: NHCO-COOR6 (wherein R6 represents a hydrogen atom or a lower alkyl group) or a residue represented by the following formula: ##STR3## have very high aldose reductase inhibitory activity and already filed a patent application (Japanese Patent Application Serial No. Hei 1-70520).
Among these chemical substances according to the present invention, [5-(2-thienyl)tetrazol-1-yl] acetic acid and ethyl ester thereof as well as [5-(2-furyl)tetrazol-1-yl] acetic acid and ethyl ester thereof are reported in an article of A. K. Zorenzen, Acta Chem. Scand., 1972, 26, p. 541. However, this article only discloses a method for preparing these substances, but there is no disclosure about the biological activity thereof.
Accordingly, an object of the present invention is generally to provide a compound which shows excellent aldose reductase inhibitory activity, has low toxicity to organisms and is quite effective as a preventive medicine and/or remedy for diabetic complications and more specifically to provide a tetrazoleacetic acid derivative.
Another object of the present invention is to provide an aldose reductase inhibitor which comprises the tetrazoleacetic and derivative as an effective component ane which is effective as a preventive medicine and/or remedy for diabetic complications.
A further object of the present invention is to provide a method for alleviating or reducing symptoms related to diabetic complications.
According to an aspect of the present invention, there is provided a novel tetrazoleacetic acid derivative represented by the following general formula (I): ##STR4## [in Formula (I), R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralky group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] except for [5-(2-thienyl)tetrazol-1-yl] acetic acid, [5-(2-furyl)tetrazol-1-yl] acetic acid, (5-(5-bromo-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylthio-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylsulfonyl-2-furyl)tetrazol-1-yl)acetic acid and ethyl ester thereof or a salt thereof.
According to another aspect of the present invention, there is provided in aldose reductase inhibitor which comrpises a tetrazoleacetic acid derivative represented by the following general formul (II): ##STR5## [in Formula (II), R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] or a salt thereof and a pharmaceutical acceptable carrier.
According to a further aspect of the present invention, there is provided a method for alleviating or reducing diabetic complications wherein a tetrazoleacetic acid derivative represented by the following general formula (II): ##STR6## [in Formula (II), R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents --O-- or --S--] or a salt thereof is used.
The tetrazoleacetic acid derivatives and the aldose reductase inhibitor as well as the method for alleviating diabetic complications according to the present invention will hereunder be explained in more detail.
First, each substituent in Formulae (I) or (II) will be explained in detail.
The alkyl group represented by R1 or R2 is, for instance, methyl, ethyl, propyl, isopropyl, butyl, isobutyl or t-butyl group; the aralkyl group includes, for instance, phenylpropyl and benzyl group; examples of the alkoxy groups are methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy and t-butoxy groups; examples of the alkoxyalkyl groups are methoxymethyl and butoxymethyl groups; the haloalkyl groups are, for instance, mono-, di or tri-haloalkyl groups such as chloromethyl, bromomethyl, fluoromethyl and chlorobutyl groups; the alkyl or aryl thio groups are, for instance, methylthio, ethylthio, butylthio and phenylthio groups; the alkylaminosulfonyl groups include, for instance, mono- or dialkylaminosulfonyl groups such as methylaminosulfonyl, ethylaminosulfonyl, propylaminosulfonyl and butylaminosulfonyl groups; the alkyl or aryl sulfonylamino groups are, for instance, methylsulfonylamino, ethylsulfonylamino, butylsulfonylamino and phenylsulfonylamino groups; examples of the alkyl or aryl carbonylamino groups are methylcarbonylamino, ethylcarbonylamino, propylcarbonylamino and phenethylcarbonylamino groups; examples of the alkyl or aryl sulfonyl groups are methylsulfonyl, ethylsulfonyl, butylsulfonyl and piperidinosulfonyl groups; and examples of the alkyl sulfinyl groups are methylsulfinyl, ethylsulfinyl and butylsulfinyl groups. These substituents may be present on any position on the furan or thiophene ring.
In addition, salts of the foregoing compounds represented by Formulae (I) and (II) wherein R1 is a hydrogen atom are pharmaceutically acceptable ones and typical examples thereof include inorganic salts such as alkali metal salts (for instance, sodium salts and potassium salts), alkaline earth metal salts (for instance, calcium salts and magnesium salts) and ammonium salts; and organic salts such as organic amine salts (for instance, triethylamine salts, pyridine salts and ethanolamine salts) and salts with basic amino acids, for instance, arginine.
The aldose reductase inhibitors according to the present invention comprises, as an essential component, at least one compound represented by the foregoing general formula (II) and are effective as preventive medicines and/or remedies for diabetic complications. It has been known that the term "diabetic complications" means a variety of pathema such as peripheral disorder, retinopathy, nephrosis, cataract and keratopathy. These diseases or disorders are triggered by hyperglycemia resulted from the diabetic disease, that the production of sorbitol in the polyol metabolic pathway is correspondingly abnormally accelerated and that, as a result, a large amount of sorbitol is accumulated within cells. This leads to the onset of these diseases.
The aldose reductase inhibitors of the present invention can suppress the sorbitol-pproduction through strong inhibition of the activity of the aldose reductase which catalyzes the sorbitor-production in the foregoing polyol metabolic pathway and thus show excellent preventive and/or treating effects for these various diabetic complications.
The dose of the compounds of formulae (I) and (II) is appropriately determined depending on the conditions or symptoms of patients to be treated, but in general ranges from 1 to 1,000 mg per day for adult which is administered at one time or over several times. The compounds may be administered through any route for medication such as oral administration, subcutaneous injection, intravenous injection and local administration.
The aldose reductase inhibitors of the present invention may usually comprise in addition to the foregoing compounds as the essential components, pharmaceutically acceptable carriers, vehicles and other additives. the inhibitors of the invention may be used in any dosage form such as tablets, powder, fine particles, granules, capsules, pills, liquid preparations, solutions and suspension for injection and eye drops.
Then methods for preparing the compounds (I) as the essential components, conditions therefor or the like will be detailed below with reference to the following reaction schemes. ##STR7##
The reaction scheme I shows the tetrazole ring formation reaction in which N-aryloylaminoalkyl carboxylate is racted with a chlorinating agent such as phosphorus pentoxide, thionyl chloride or thionyl chloride/N,N dimethylformamide to obtain a corresponding imidoyl chloride compound and then the product is reacted with sodium azide to obtain an intended compound of Formula (I). The reaction for obtaining the imidoyl chloride can be carried out in an organic solvent such as benzene, toluene or methylene chloride. In general, the reaction is preferably performed at a temperature of not more than room temperature. In the subsequent cyclization reaction, it is preferred to use soidum azide in an amount of 2 to 6 times that of the imidoyl chloride as an intermediate. The cyclization reaction is in general performed at room temperature in N,N-dimethylformamide.
The reaction scheme 2 means that the compounds of formula (I) in which R1 is a hydrogen atom may be prepared by hydrolysis of the carboxylic acid ester obtained in the reaction scheme 1. The hydrolysis can be performed in the presence of a base such as sodium hydroxide or potassium hydroxide or an acid such as hydrochloric acid. sulfuric acid, acetic acid or trifluoroacetic acid.
The compounds of Formula (I) Prepared according to the foregoing method are separated and purified by a chemical operation commonly employed such as extraction, recrystallization and/or column chromatography and the products thus separated and purified are used as essential components for the aldose reductase inhibitors of the present invention.
The present invention will hereinafter described in more detail with reference to the following non-limitative working Examples and the effects practically achieved by the present invention will also be discussed in detail with reference to Test Examples.
PAC (1-1) preparation of methyl [5-(2-thienyl)tetrazol-1-yl]acetateTo a solution of 1 g (5.02 mM) of N-(2-thenoyl)glycine methyl ester in 15 ml of anhydrous methylene chloride, there was slowly added 1.5 g (7.2 mM) of phosphorus pentoxide at room temperature with stirring, the resulting mixture was stirred for additional 30 minutes and the reaction solumtion was concentrated at 40°C under reduced pressure. The resulting residue was dissolved in 5 ml of N,N-dimethylformamide. The solution was dropwose added to a suspension of 1.6 g (24.6 mM) of sodium azide in 3 ml of N,N-dimethylformamide at room temperature over 30 minutes with stirring. After the dropwise addition and agitation for additional 30 minutes at room temperature, the mixture was poured into ice-water and extracted with ethyl acetate. The organic phase obtained was washed with water, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant residue was subjected to silica gel column chromatography (eluent: ethyl acetate/benzene=1/20) for separation and purification to thus give 0.59 g (yield 52.4%) of methyl (5-(2-thienyl)tetrazol-1-yl] acetate.
M.P.=73-74°C
N.M.R. (CDCl3) δppm: 3.84 (s, 3H); 5.34 (s, 2H); 7.24 (dd, 1H, J=5.20, 3.60 Hz); 7.58 (dd, 1H, J=3.60, 1.20 Hz); 7.65 (dd, 1H, J=5.20, 1.20 Hz).
I.R. νKBr (cm-1): 3400, 1730, 1650, 1540, 1370, 1230.
Mass: m/z 224 [M+ ]
The following compounds were prepared in the same manner used in Example (1-1)
Starting material: N-(3-methyl-2-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 2.43 (s, 3H); 3.80 (s, 3H); 5.25 (s, 2H); 7.07 (d, 1H, J=5.0 Hz); 7.52 (d, 1H, J=5.0 Hz).
I.R. νNaCl (cm-1): 3100, 2950, 1760, 1440, 1220, 1000.
Mass: m/z 238 [M+ ]
Starting material: N-(4-methyl-2-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δpm: 2.34 (s, 3H); 3.83 (s, 3H); 5.33 (s, 2H); 7.22 (d, 1H, J=1.2 Hz); 7.41 (d, 1H, J=1.2 Hz).
I.R. νNaCl (cm-1): 3090, 2950, 1740, 1580, 1440, 1240.
Mass: m/z 238 [M+ ]
Starting material: N (5-methyl-2-thenoyl)glycine methyl ester
M.P.=88-89°C
N.M.R. (CDCl3) δppm: 2.57 (s, 3H): 3.83 (s, 3H); 5.32 (s, 2H); 6.87∼6.89 (m, 1H); 7.36∼7.39 (m, 1H).
I.R. νKBr (cm-1): 3440, 1750, 1580, 1510, 1430, 1260, 1230, 1100.
Mass: m/z 238 [M+ ]
Starting material: N-(3-thenoyl)glycine methyl ester
M.P.=106-107°C
N.M.R. (CDCl3) δppm: 3.84 (s, 3H); 5.27 (s, 2H); 7.48 (dd, 1H, J=5.01, 1.20 Hz); 7.56 (dd, 1H, J=5.01, 2.80 Hz); 8.25 (dd, 1H, J=2.80, 1.20 Hz)
I.R. νKBr (cm-1): 3100, 1760, 1580, 1440, 1360, 1230.
Mass m/z 224 [M+ ]
Starting material: N-(2-furoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 3.79 (s, 3H); 5.49 (s, 2H); 6.66 (dd, 1H, J=3.60, 2.01 Hz); 7.36 (dd, 1H, J=3.60, 0.80 Hz); 7.64 (dd, 1H, J=2.01, 0.80 Hz)
I.R. νNaCl (cm-1): 3120, 3000, 2950, 1750, 1620, 1520, 1440, 1220, 1010.
Mass: m/z 208 M+ ]
Starting material: N-(3-furoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 3.84 (s, 3H); 5.24 (s, 2H); 6.81 (bs, 1H); 7.63 (bs, 1H); 7.96 (bs, 1H)
I.R. νNaCl (cm-1): 3140, 2950, 1750, 1440, 1220.
Mass: m/z 208 [M+ ]
Starting material: N-(5-ethyl-2-thenoyl)glycine methyl ester
M.P.=45-46°C
N.M.R. (CDCl3) δppm: 1.36 (t, 3H, J=7.70 Hz); 2.91 (dq, 2H, J=7.70, 0.80 Hz); 3.83 (s, 3H); 5.32 (s, 2H); 6.91 (dt, 1H, J=3.60, 0.80 Hz); 7.40 (d, 1H, J=3.60 Hz)
I.R. νKBr (cm-1): 2960, 1760, 1580, 1510, 1430, 1270, 1220, 1100, 1000, 820.
Mass: m/z 252 [M+ ]
Starting material: N-(5-benzyl-2-thenoyl)glycine methyl ester
M.P.=71-72°C
N.M.R. (CDCl3) δppm: 3.80 (s, 3H); 4.20 (s, 2H); 5.29 (s, 2H); 6.91 (dt, 1H, J=4.01, 1.20 Hz); 7.23∼7.38 (m, 5H); 7.39 (d, 1H, J=4.01 Hz)
I.R. νKBr (cm-1): 3000, 1740, 1580, 1510, 1460, 1420, 1380, 1270, 1240, 800.
Mass: m/z 314 [M+ ]
Starting material: N-(5-methylthio-2-thenoyl)glycine methyl ester
M.P.=64-65°C
N.M.R. (CDCl3) δppm: 2.60 (s, 3H); 3.84 (s, 3H); 5.31 (S, 2H); 7.07 (d, 1H, J=4.00 Hz); 7.45 (d, 1H, J=4.00 Hz)
I.R. νKBr (cm-1): 3470, 1750, 1580, 1480, 1440, 1410, 1360, 1260, 1220, 1100, 990, 790.
Mass: m/z 270 [M+ ]
Starting material: N-(5-bromo-2-thenoyl)glycine methyl ester
M.P.=45-46°C
N.M.R. CDCl3) δppm: 3.84 (s, 3H); 5.30 (s, 2H); 7.19 (d, 1H, J=4.90 Hz); 7.30 (d, 1H, J=4.90 Hz)
I.R. νKBr (cm-1): 3450, 1740, 1580, 1490, 1440, 1400, 1270, 1240, 1100, 980, 800.
Mass: m/z 303 [M+ ]
Starting material: N-(2-bromo-3-thenoyl)glycine methyl ester
N.M.R. CDCl3) δppm: 2.58 (s, 3H); 3.80 (s, 3H); 5.12 (s, 2H, 6.99 (d, 1H, J=5.20 Hz); 7.27 (d, 1H, J=5.20 Hz)
I.R. νNaCl (cm-1): 2950, 1750, 1580, 1500, 1440, 1260, 1220.
Mass: m/z 238 [M+ ]
Starting material: N-(5-bromomethyl-2-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 2.49 (s, 3H); 3.85 (s, 3H); 5.30 (s, 2H); 7.26∼7.36 (m, 2H).
I.R. νNaCl (cm-1): 2950, 1760, 1580, 1500, 1440, 1270, 1220, 1000, 800.
Mass: m/z 317 [M+ ]
Starting material: N-(5-phenyl-2-thenoyl)glycine methyl ester
M.P.=133-134°C
N.M.R. (CDCl3) δppm 3.85 (s, 3H); 5.38 (s, 2H); 7.39 (d, 1H, J=3.80 Hz); 7.40∼7.48 (m, 3H); 7.55 (d, 1H, J=3.80 Hz); 7.63∼7.66 (m, 2H).
I.R. νKBr (cm-1); 3440, 1760, 1580, 1480, 1420, 1220, 750.
Mass: m/z 300 [M+ ]
Starting material: N-(3-methylcarbonylamino-2-thenoyl)glycine methyl ester
M.P. 35-36°C
N.M.R. (CDCl3) δppm: 2.31 (s, 3H); 3.84 (s, 3H); 5.45 (s, 2H); 7.56 (d, 1H, J=5.20 Hz); 8.34 (d, 1H, J=5.20 Hz).
I.R. νKBr (cm-1): 3240, 1750, 1580, 1490, 1440, 1220, 1180, 930, 750.
Mass: m/z 281 [M+ ]
Starting material: N-(3-propylcarbonylamino-2-thenoyl)glycine methyl ester
M.P.=92-93°C
N.M.R. (CDCl3) δppm: 1.04 (t, 3H, J=7.3 Hz); 1.76∼1.90 (m, 2H); 2.51 (t, 3H, J=7.30 Hz); 3.84 (s, 3H); 5.46 (s, 2H); 7.56 (d, 1H, J=5.50 Hz); 8.37 (d, 1H, J=5.50 Hz); 10.75 (bs, 1H).
I.R. νKBr (cm-1): 3270, 2940, 1740, 1680, 1580, 1410, 1380, 1260, 1240, 1100, 760
Mass: m/z 309 [M+ ]
Starting material: N-(3-phenethylcarbonylamino-2-thenoyl)glycine methyl ester
M.P.=96-97°C
N.M.R. (CDCl3) δppm: 2.85 (t, 2H, J=7.70 Hz); 3.11 (t, 2H, J=7.70 Hz); 3.82 (s, 3H); 5.43 (s, 2H); 7.18∼7.30 (m, 5H); 7.55 (d, 1H, J=5.50 Hz); 8.34 (d, 1H, J=5.50 Hz); 10.75 (bs, 1H).
I.R. νKBr (cm-1): 3300, 1760, 1700, 1580, 1440, 1390, 1220, 1100.
Mass: m/z 371 .[M+ ]
Starting material: N-(5-methyl-2-furoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 2.39 (d, 3H, J=0.98 Hz); 3.80 (s, 3H); 5.45 (s, 2H); 6.25 (dq, 1H, J=3.66, 0.98 Hz); 7.23 (d, 1H, J=3.66 Hz).
I.R. νNaCl (cm-1): 3120, 2950, 1740, 1620, 1570, 1440, 1220, 1020, 790.
Mass: m/z 222 [M+ ]
Starting material: N-(5-5butyl-2-furoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 0.95 (t, 3H, J=7.33 Hz); 1.31∼1.45 (m, 2H); 1.57∼170 (m, 2H); 2.70 (t, 2H, J=7.57 Hz); 3.79 (s, 3H); 5.45 (s, 2H); 6.24 (d, 1H, J=3.66 Hz); 7.24 (d, 1H, J=3.66 Hz).
I.R. νNaCl (cm -1): 2950, 1760, 1620, 1560, 1440, 1220, 1020, 790.
Mass m/z 264 [M+ ]
Starting material: N-(5-bromo-2-furoyl)glycine methyl ester
M.P.=106-107°C
N.M.R. (CDCl3) δppm: 3.84 (s, 3H); 5.45 (s, 2H); 6.58 (d, 1H, J=3.54 Hz); 7.31 (d, 1H, J=3.54 Hz).
I.R. νKBr (cm-1): 3100, 3000, 1730, 1620, 1520, 1440, 1280, 1100, 1000, 780.
Mass: m/z 287 [M+ ]
Starting material: N-(5-methylthio-2-furoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 2.48 (s, 3H); 3.82 (s, 3H); 5.47 (s, 2H); 6.55 (d, 1H, J=3.66 Hz); 7.32 (d, 1H, J=3.66 Hz).
I.R. νNaCl (cm-1): 3100, 2950, 1750, 1610, 1500, 1440, 1220, 1100, 1010, 780.
Mass: m/z 254 [M+ ]
Starting material: N-(2-bromo-3-furoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 3.81 (s, 3H); 5.23 (s, 2H);6.70 (d, 1H, J=2.20 Hz); 7.52 (d, 1H, J=2.20 Hz).
I.R. νNaCl (cm-1): 3150, 2950, 1750, 1620, 1530, 1440, 1220, 960.
Mass: m/z 287 .[M+ ]
Starting material: N-[2(-oct-4-yl)-3-furoyl] glycine methyl ester
N.M.R. (CDCl3) δppm: 0.82 (t, 6H, J=7.20 Hz); 1.10∼1.27 (m, 6H): 1.52∼1.70 (m, 4H); 3.25∼3.31 (m, 1H); 3.81 (s, 3H); 5.16 (s, 2H); 6.40 (d, 1H, J=2.20 Hz); 7.48 (d, 1H, J=2.20 Hz).
I.R. νNaCl (cm-1): 2950, 2850, 1750, 1620, 1530, 1440, 1220, 1000, 960.
Mass: m/z 320 [M+ ]
Starting material: N-[2-methylthio-3-furoyl)glycine methyl ester
M.P.=71-72°C
N.M.R. (CDCl3)δppm: 2.51 (s, 3H); 3.78 (s, 3H); 5.25 (s, 2H); 6.65 (d, 1H, J=2.20 Hz); 7.63 (d, 1H, J=2.20 Hz).
I.R. νNaCl (cm-1): 3150, 2950, 1750, 1600, 1530, 1430, 1220, 960, 740.
Mass: m/z 254 [M+ ]
Starting material: N-(3-methylsulfonylamino-2-thenoyl)glycine methyl ester
M.P.=154-155°C
N.M.R. (CDCl3) δppm: 3.01 (s, 3H); 3.78 (s, 3H); 5.38 (s, 2H); 7.52 (d, 1H, J=5.61 Hz); 7.55 (d, 1H, J=5.61 Hz); 9.92 (bs, 1H).
I.R. νKBr (cm-1): 3150, 3100, 1740, 1560, 1370, 1220, 1150, 760.
Mass: m/x 317 [M+ ]
Starting material: N-(3-butylsulfonylamino-2-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 0.87 (t, 3H, J=7.32 Hz); 1.35∼1.44(m, 2H); 1.57∼1.75 (m, 2H); 3.14 (t, 2H, J=7.94 Hz); 3.84 (s, 3H); 5.45 (s, 2H); 7.54 (d, 1H, J=5.49 Hz); 7.62 (d, 1H, J=5.49 Hz); 9.98 (bs, 1H).
I.R. νNaCl (cm-1): 3100, 1750, 1560, 1370, 1220, 1150
Mass: m/z 359 [M+ ]
Starting material: N-(3-phenylsulfonylamino-2-thenoyl)glycine methyl ester
M.P.=124-125°C
N.M.R. (CDCl3) δppm: 3.72 (s, 3H); 5.23 (s, 2H); 7.31∼7.47 (m, 5H); 7.53 (d, 1H, J=5.62 Hz); 7.58∼7.91 (m, 2H); 10.16 (bs, 1H).
I.R. νKBr (cm-1): 3120, 2950, 1750, 1560, 1520, 1430, 1380, 1240, 1160, 760, 580.
Mass: m/z 379 [M+ ]
Starting material: N-(2-methyl-3-furoyl)glycine methyl ester
M.P.=54.5-56°C
N.M.R. (CDCl3) δppm: 2.58 (s, 3H); 3.82 (s, 3H); 5.19 (s, 2H); 6.44 (d, 1H, J=2.00 Hz); 7.45 (d, 1H, J=2.00 Hz).
I.R. νKBr (cm-1): 3410, 3150, 1760, 1620, 1540, 1460, 1370, 1230.
Mass: m/z 222 [M+ ]
Starting material: N-[5- [N'-methyl-N'- [2-(methoxymethoxy)ethyl]-aminosulfonyl]-2-thienoyl)] glycine methyl ester
N.M.R. (CDCl3) δppm: 2.77 (s, 3H); 3.14 (t, 2H, J=5.37 Hz); 3.32 (s, 3H); 3.59 (t, 2H, J=5.37 Hz); 3.72 (s, 3H); 4.56 (s, 2H; 5.21 (s, 2H); 7.25 (d, 1H, J=5.13 Hz); 7.71 (d, 1H, J=5.13 Hz).
I.R. νKBr (cm-1): 2950, 1750, 1440, 1350, 1220, 1150, 1040, 750, 710.
Mass: m/z 405 [M+ ]
PAC (2-1) [5-(2-thienyl)tetrazol-1-yl ] acetic acid0.5 g (2.2 mM) of methyl [5-(2-thienyl)tetrazol-1-yl) acetate obtained in Example (1-1) was dissolved in 3 ml of methanol, 1 ml of a 4 N aqueous sodium hydroxide solution was added to the resulting solution at room temperature and the mixture was refluxed with heating for one hour. After cooling the mixture to room temperature, it was diluted with water, then impurities were removed with ethyl acetate and the aqueous phase was separated. The aqueous phase was acidified with hydrochloric acid, crystals precipitated out were filtered off, washed with water and recrystallized from a 50% ethanol-water mixture to give 0.39 g (yield 84.4%) of [5-(2-thienyl)tetrazol-1-yl] acetic acid.
M.P.=129-130°C (decomposition)
N.M.R. (DMSO-d6) δppm: 4.9∼6.2 (br, 1H); 5.30 (s, 3H); 7.27∼7.33 (m, 1H); 7.61 (dd, 1H, J=3.60, 1.20 Hz): 7.68 (dd, 1H, J=3.60, 1.20 Hz).
I.R. νKBr (cm-1): 3380, 1730, 1580, 1350, 1250.
Mass: m/z 210 [M+ ]
The following compounds were prepared in the same manner used in Example (2-1)
Starting Material: methyl [5-(3-methyl-2-thienyl)tetrazol-1-yl] acetate
M.P.=165-166°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.42 (s, 3H); 3.70 (bs, 1H); 5.20 (s, 2H); 7.06 (d, 1H, J=5.2 Hz); 7.53 (d, 1H, J=5.2 Hz).
I.R. νKBr (cm-1): 3100, 2500, 1720, 1570, 1510, 1420, 1220.
Mass: m/z 224 [M+ ]
Starting Material: methyl [5-(4-methyl-2-thienyl)tetrazol-1-yl] acetate
M.P.=154-155°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.34 (s, 3H); 5.29 (bs, 3H); 7.22 (d, 1H, J=1.2 Hz); 7.41 (d, 1H, J=1.2 Hz).
I.R. νKBr (cm-1): 3500, 2550, 1730, 1520, 1450, 1270, 1240, 1120.
Mass: m/z 224 [M+ ]
Starting Material: methyl. [5-(5-methyl-2-thienyl)tetrazol-1-yl] acetate
M.P.=150-151°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.58 (s, 3H); 5.28 (s, 2H); 5.90 (bs, 1H); 6.88∼6.92 (m, 1H); 7.39∼7.42 (m, 1H).
I.R. νKBr (cm-1): 3400, 2990, 1730, 1580, 1520, 1440, 1260, 1240, 1000.
Mass: m/z 224 [M+ ]
Starting Material: methyl [5-(3-thienyl)tetrazol-1-yl] acetate
M.P.=172-173°C (decomposition)
N.M.R. (DMSO-d6) δppm: 3.33 (bs, 1H); 5.58 (s, 2H); 7.57-(dd, 1H, J=5.20, 1.20 Hz); 7.85 (dd, 1H, J=5.20, 2.80 Hz); 8.25 (dd, 1H, J=2.80, 1.20 Hz).
I.R. νKBr (cm-1): 3380, 3120, 1730, 1580, 1280.
Mass: m/z 210 [M+ ]
Starting Material: methyl [5-(2-furyl)tetrazol-1-yl] acetate
M.P.=157-158°C (decomposition)
N.M.R. (CDCl3 -DMSO-d6) δppm: 4.79 (bs, 1H); 5.45 (s, 2H); 6.81 (dd, 1H, J=3.60, 1.60 Hz); 7.37 (d, 1H, J=3.6 Hz); 8.08 (d, 1H, J=1.70 Hz).
I.R. νKBr (cm-1): 3010, 2970, 2520, 1730, 1620, 1520, 1220, 1020.
Mass: m/z 194 [M+ ]
Starting Material: methyl [5-(3-furyl)tetrazol-1-yl] acetate
M.P.=150-151°C (decomposition)
N.M.R. (DMSO-d6) δppm: 3.33 (bs, 1H); 5.56 (s, 2H); 7.00 (bs, 1); 7.97 (bs, 1H); 8.46 (bs, 1H).
I.R. νKbr (cm-1): 3370, 2430, 1720, 1620, 1350, 1240.
Mass: m/z 194 [M+ ]
Starting Material: methyl [5-(5-ethyl 2-thienyl)tetrazol-1-yl] acetate
M.P.=131-138°C
N.M.R. (DMSO-d6) δppm: 1.36 (dt, 3H, J=7.70, 1.20 Hz); 2.93 (q, 2H, J=7.70 Hz); 3.28 (bs, 1H); 5.28 (s, 2H); 6.92 (dd, 1H, J=3.60, 1.20 Hz); 7.41 (dd, 1H, J=3.60, 1.20 Hz).
I.R. νKBr (cm-1): 3490, 2950, 1740, 1580, 1500, 1410, 1220, 1110, 800.
Mass m/z 238 . [M+ ]
Starting Material: methyl [5-(5-benzyl-2-thienyl)tetrazol-1-yl] acetate
M.P.=148-149°C
N.M.R. (DMSO-d6) δppm: 4.02 (s, 2H); 4.70 (bs, 1H); 5.25 (s, 2H); 6.92 (dd, 1H, J=3.60, 0.80 Hz); 7.23∼7.38 (m, 5H); 7.41 (d, 1H, J=3.60).
I.R. (cm-1): 2950, 1750, 1580, 1510, 1430, 1230.
Mass: m/z 300 [M+ ]
Starting Material: methyl [5-(5-methylthio-2-thienyl)tetrazol-1-yl ] acetate
M.P.=179°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.61 (s, 3H); 5.34 (s, 2H); 7.10 (d, 1H, J=4.01 Hz); 7.49 (d, 1H, J=4.01 Hz).
I.R. νKBr (cm-1): 3400, 1730, 1570, 1480, 1410, 1210.
Mass: m/z 256 [M+ ]
Starting Material: methyl. [5-(5-bromo-2-thienyl)tetrazol-1-yl] acetate
M.P.=200°C (decomposition)
N.M.R. (DMSO-d6) δppm: 5.30 (s, 2H); 6.63 (bs, 1H); 7.19 (d, 1H, J=4.01 Hz); 7.34 (d, 1H, J=4.01 Hz).
I.R. νKBr (cm-1): 3100, 2900, 1730, 1580, 1490, 1440, 1400, 1280, 1260, 1100, 980, 880. 800.
Mass: m/z 289 [M+ ]
Starting Material: methyl [5-(2-methyl-3-thienyl)tetrazol1-yl] acetate
M.P.=144°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.57 (s, 3H); 5.08 (s, 2H); 7.06 (d, 1H, J=5.20 Hz); 7.27 (d, 1H, J=5.20 Hz).
I.R. νKBr (cm-1): 2900, 1740, 1570, 1440, 1400, 1340, 1260, 1220.
Mass: m/z 224 [M+ ]
Starting Material: methyl [5-(5-bromomethyl-2-thienyl)tetrazol-1-yl] acetate
M.P.=192°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.49 (s, 3H); 4.62 (bs, 1H); 5.28 (s, 2H); 7.39∼7.41 (m, 2H).
I.R. νKBr (cm-1): 3000, 1740, 1500, 1240, 1140.
Mass: m/z 303 [M+ ]
Starting Material: methyl [5-(5-phenyl-2-thienyl)tetrazol-1-yl] acetate
M.P.: 210°C (decomposition)
N.M.R. (DMSO-d6) δppm: 4.03 (bs, 1H); 5.36 (s, 2H) 7.36∼7.48 (m, 3H); 7.42 (d, 1H, J=4.01 Hz); 7.58 (d, 1H, J=4.01 Hz); 7.64∼7.67 (m, 2H).
I.R. νKBr (cm-1): 3000, 1730, 1580, 1480, 1430, 1240, 1110, 760.
Mass: m/z 286 [M+ ]
Starting Material: methyl [5-(3-methoxy-2-thienyl)tetrazol-1-yl] acetate
M.P.: 234°C (decomposition)
N.M.R. (DMSO-d6) δppm: 3.94 (s, 3H); 5.36 (s, 2H); 6.95 (d, 1H, J=5.50 Hz); 7.55 (d, 1H, J=5.50 Hz).
I.R. νKBr (cm-1): 3110, 2950, 1740, 1580, 1520, 1440, 1250, 1200, 1070, 800, 750.
Mass: m/z 240 [M+ ]
Starting Material: methyl [5-(3-butoxy-2-thienyl)tetrazol-1-yl] acetate
M.P.: 197-198°C (decomposition)
N.M.R. (DMSO-d6) δppm: 0.95 (t, 3H, J=7.30 Hz); 1.34∼1.41 (m, 2H); 1.70∼1.81 (m, 2H); 4.13 (t, 2H, J=6.60 Hz); 4.80 (bs, 1H); 5.35 (s, 2H); 6.94 (d, 1H, J=5.50 Hz); 7.54 (d, 1H, J=5.50 Hz).
I.R. νKBr (cm-1): 3500, 2950, 1730, 1570, 1510, 1400, 1250, 1200, 1070, 800, 750.
Mass: m/s 282 [M+ ]
Starting Material: methyl [5-(3-methylcarbonylamino-2-thienyl)-tetrazol-1-yl] acetate
M.P.: 221°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.92 (s, 3H); 3.80∼4.80 (br, 1H); 5.42 (s, 2H); 7.59 (d, 1H, J=5.40 Hz); 8.28 (d, 1H, J=5.40 Hz).
I.R. νKBr (cm-1): 3250, 2920, 1740, 1650, 1580, 1440, 1390, 1240, 1220, 1110, 760.
Mass: m/z 267 [M+ ]
Starting Material: methyl [5-(3-propylcarbonylamino 2-thienyl)-tetrazol-1-yl] acetate
M.P.: 192°C (decomposition)
N.M.R. (DMSO-d6) δppm: 1.03 (t, 3H, J=7.30 Hz); 1.74∼1.88 (m, 2H); 2.19 (t, 2H, J=7.30 Hz); 4.40∼5.60 (br, 1H); 5.41 (s, 2H); 7.59 (d, 1H, J=5.50 Hz); 8.30 (d, 1H, J=5.50 Hz); 10.74 (bs, 1H).
I.R. νKBr (cm-1): 3310, 2960, 1720, 1590, 1530, 1440, 1180, 760.
Mass: m/z 295 [M+ ]
Starting Material: methyl [5-(3-phenethylcarbonylamino-2-thienyl) tetrazol-1-yl] acetate
M.P.: 178°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.83 (t, 2H, J=7.70 Hz); 3.09 (t, 2H, J=7.70 Hz); 4.22 (bs, 1H); 5.39 (s, 2H); 7.18∼7.30 (m, 5H); 7.60 (d, 1H, J=5.50 Hz); 8.27 (d, 1H, J=5.50 Hz); 10.72 (bs, 1H).
I.R. νKBr (cm-1); 3450, 2920, 1740, 1640, 1580, 1440, 1400, 1220, 1110.
Mass: m/z 357 [M+ ]
Starting Material: methyl [5-(5-butyl-2-thienyl)tetrazol-1-yl] acetate
M.P.: 103-104°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 0.95 (t, 3H, J=7.33 Hz); 1.35∼1.49 (m, 2H); 1.65∼1.76 (m, 2H); 2.89 (t, 2H, J=7.33 Hz); 5.27 (s, 2H); 6.89 (d, 1H, J=3.66 Hz); 7.41 (d, 1H, J=3.66 Hz).
I.R. νKBr (cm-1): 2920, 1730, 1580, 1520, 1420, 1220, 800.
Mass: m/z 266 [M+ ]
Starting Material: methyl [5-(5-phenylpropyl 2-thienyl)-tetrazol-1-yl] acetate
M.P.: 85-86°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 2.06 (quint., 2H, J=7.57 Hz); 2.71 (t, 2H, J=7.57 Hz); 2.91 (t, 2H, J=7.57 Hz); 4.98 (bs, 1H; 5.28 (s, 2H); 6.91 (d, 1H, J=3.80 Hz); 7.18∼7.33 m, 5H); 7.42 (d, 1H, J=3.80 Hz).
I.R. νKBr (cm-1): 2920, 1720, 1580, 1510, 1420, 1220, 1130, 800.
Mass: m/z 328 [M+ ]
Starting Material: methyl [5-(5-methoxymethyl-2-thienyl)-tetrazol-1-yl] acetate
M.P.: 124-125°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 3.43 (s, 3H); 4.67 (d, 2H, J=0.73 Hz); 5.29 (s, 2H); 7.10 (dt, 1H, J=3.66, 0.73 Hz); 7.49 (d, 1H, J=3.66 Hz).
I.R. νKBr (cm-1): 2900, 1740, 1580, 1420, 1220, 1020, 800.
Mass: m/z 254 [M+ ]
Starting Material: methyl [5-(5-butoxymethyl-2-thienyl)-tetrazol-1-yl] acetate
M.P.: 67-68°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 0.93 (t, 3H, J=7.20 Hz); 1.38∼1.47 (m, 2H); 1.55∼1.66 (m, 2H); 3.54 (t, 2H, J=6.47 Hz); 4.67 (d, 2H, J=0.73 Hz); 4.07 (s, 2H); 5.27 (s, 2H); 7.07 (d, 1H, J=3.79 Hz); 7.47 (d, 1H, J=3.79 Hz).
I.R. νKBr (cm-1): 2950, 1730, 1580, 1420, 1230, 1090, 800.
Mass: m/z 296 [M+ ]
Starting Material: methyl [5-(2-bromo-3-thienyl)tetrazol-1-yl] acetate
M.P.: 145-146°C
N.M.R. (CDCl3+DMSO-d6) δppm: 4.56 (bs, 1H); 5.10 (s, 2H); 7.12 (d, 1H, J=5.18 Hz); 7.47 (d, 1H, J=5.18 Hz).
I.R. νKBr (cm-1): 2950, 1740, 1570, 1440, 1220, 1000, 800, 720.
Mass: m/z 289 [M+ ]
Starting Material: methyl [5-[2-(oct-4-yl)-3-thienyl] tetrazol-1-yl] acetate
M.P.: 79-80°C
N.M.R. (CDCl3+DMSO-d6) δppm: 0.78∼0.84 (m, 6H); 1.13∼1.25 (m, 6H); 1.45∼1.71 (m, 4H); 3.15∼3.22 (m, 1H); 5.00 (s, 2H); 7.01 (d, 1H, J=5.37 Hz); 7.36 (dd. 1H, J=5.37, 0.73 Hz).
I.R. νKBr (cm-1): 2900, 1740, 1570, 1110, 1220, 720.
Mass: m/z 322 . [M+ ]
Starting Material: methyl [5-(2-methylthio-3-thienyl)-tetrazol-1-yl] acetate
M.P.: 134-135°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 2.51 (s, 3H); 5.14 (s, 2H); 7.18 (d, 1H, J=5.50 Hz); 7.47 (d, 1H, J=5.50 Hz).
I.R. νKBr (cm-1): 3100, 2900, 1730, 1550, 1440, 1220, 800,
Mass: m/z 256 [M+ ]
Starting Material: methyl [5-(5-methyl-2-furyl)tetrazol-1-yl] acetate
M.P. 150-151°C (decomposition)
N.M.R. (CDCl3 +DMSO-d6) δppm: 2.41 (s, 3H); 5.40 (s, 2H); 6.23 (dd, 1H, J=3.42, 0.98 Hz); 7.20 (d, 1H, J=3.42 Hz).
I.R. νKbr (cm-1): 3500, 3100, 1720, 1570, 1440, 1240, 800.
Mass: m/z 208 [M+ ]
Starting Material: methyl. [5-(5-butyl-2-furyl)tetrazol-1-yl] acetate
M.P.: 109-110°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 0.95 (t, 3H, J=7.20 Hz); 1.32∼1.46 (m, 2H); 1.62∼1.73 (m, 2H); 2.72 (t, 2H, J=7.56 Hz); 5.40 (s, 2H); 6.24 (d, 1H, J=3.42 Hz); 7.19 (d, 1H, J=3.42 Hz).
I.R. νKBr (cm-1): 2900, 1740, 1560, 1450, 1200, 800.
Mass: m/z 250 [M+ ]
Starting Material: methyl [5-(5-bromo-2-furyl)tetrazol-1-yl] acetate
M.P.: 159-160°C (decomposition)
N.M.R. (CDCl3 +DMSO-d6) δppm: 5.41 (s, 2H); 6.60 (d, 1H, J=3.66 Hz); 7.27 (d, 1H, J=3.66 Hz).
I.R. νKBr (cm-1): 3150, 3000, 1730, 1600, 1420, 1200, 740.
Mass: m/z 273 [M+ ]
Starting material: methyl [5-(5-methylthio-2-furyl)tetrazol-1-yl] acetate
M.P.: 160.5-161.5°C (decomposition)
N.M.R. (CDCl3 +DMSO-d6) δppm: 2.51 (s, 3H); 5.43 (s, 2H); 6.55 (d, 1H, J=3.66 Hz); 7.28 (d, 1H, J=3.66 Hz).
I.R. νKBr(cm-): 3100, 3000, 1730, 1620, 1500, 1440, 1210, 1200, 800.
Mass: m/z 240 [M+ ]
Starting Material: methyl [5-(2-bromo-3-furyl)tetrazol-1-yl] acetate
M.P.: 138-139°C (decomposition)
I.R. (CDCl3 +DMSO-d6) δppm: 5.17 (s, 2H); 4.33 (bs, 1H); 6.74 (d, 1H, J=2.20 Hz); 7.54 (d, 1H, J=2.20 Hz).
I.R. νKBr (cm-1): 3100, 3000, 1720, 1620, 1520, 1440, 1260, 1100, 1010, 930
Mass m/z 273 [M+ ]
Starting Material: methyl [5-(2-methylthio-3-furyl)tetrazol-1-yl] acetate
M.P.: 120-122°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 2.53 (s, 3H); 4.09∼4.65 (br, 1H); 5.43 (s, 3H); 6.71 (d, 1H, J=1.95 Hz); 7.67 (d, 1H, J=1.95 Hz).
I.R. νKBr (cm-1): 3300, 3150, 2950, 1730, 1590, 1440, 1220, 960, 810, 740.
Mass: m/z 240 [M+ ]
Starting Material: methyl [5-(2-phenylthio-3-thienyl)tetrazol-1-yl] acetate
M.P.: 133-134°C (decomposition)
N.M.R. (CDCl3 +DMSO-d6) δppm: 5.50 (s, 2H); 7.23∼7.29 (m, 6H); 7.59 (d, 1H, J=5.30 Hz).
I.R. νKBr (cm-1): 3100, 3000, 1720, 1570, 1480, 1430, 1390, 1260, 870, 730.
Mass: m/z 318 [M+ ]
(2-34) [5-(5-phenylthio-2-thienyl)tetrazol-1-yl ] acetic acid (yield=61.0%)
Starting Material: methyl [5-(5-phenylthio-2-thienyl)tetrazol-1-yl] acetate
M.P.: 125-126°C (decomposition)
N.M.R. (CDCl3 +DMSO-d6) δppm: 3.37 (bs, 1H); 5.29 (s, 2H); 7.27∼7.38 (m, 6H); 7.51 (d, 1H, J=3.90 Hz).
I.R. νKBr (cm-1): 3000, 1730, 1580, 1480, 1430, 1410, 1220, 1130, 800, 730.
Mass m/z 318 [M+ ]
Starting Material: methyl [5- [5-(N,N-diethylaminosulfonyl)-2-thienyl] tetrazol-1-yl ] acetate
M.P.: 134-135°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 1.01 (t, 6H, J=7.08 Hz); 3.10 (q, 4H, J=7.08 Hz); 3.32 (bs, 1H); 5.25 (s, 2H); 7.23 (d, 1H, J=5.13 Hz); 8.18 (d, 1H, J=5.13 Hz).
I.R. νKBr (cm-1): 3100, 2970, 1740, 1410, 1360, 1220, 1150, 940, 700, 590.
Mass: m/z 333 [m+ ]
Starting Material: methyl [5-[5-(N,N-dibutylaminosulfonyl)-2-thienyl] tetrazol-1-yl] acetate
N.M.R. (CDCl3) δpmm: 0.79 (t, 6H, J=7.32 Hz); 1.09∼1.23 (m, 4H); 1.30∼1.41 (m, 4H); 2.87 (t, 4H), J=7.57 Hz); 5.14 (s, 2H); 7.11 (d, 1H, J=5.12 Hz); 7.61 (d, 1H, J=5.12 Hz).
I.R. νNaCl (cm-1): 2950, 1740, 1340, 1220, 1150.
Mass: m/z 401 [M+ ]
Starting Material: methyl [5-(5-piperidinosulfonyl-2-thienyl)-tetrazol-1-yl ] acetate
M.P.: 143-146°C
N.M.R. (CDCl3) δppm: 1.38∼1.39 (m, 2H); 1.48∼1.58 (m, 4H); 2.86 (t, 4H, J=5.37 Hz); 5.15 (s, 2H); 7.16 (d, 1H, J=5.13 Hz); 7.66 (d, 1H, J=5.13 Hz).
I.R. νKbr (cm-1): 3450, 2950, 1735, 1340, 1230, 1160.
Mass: m/z 357 [M+ ]
Starting Material: methyl [5- [2-(N,N-diethylaminosulfonyl)-5-trimethylsilyl-3-thienyl] tetrazol-1-yl] acetate
M.P.: 128.5-130°C
N.M.R. (CDCl3) δppm: 1.00 (t, 6H, J=7.08 Hz); 3.00 (q, 4H, J=7.08 Hz): 5.13 (s, 2H); 7.10 (d, 1H, J=4.88 Hz); 7.62 (d, 1H, J=4.88 Hz).
I.R. νKBr (cm-1): 2950, 1740, 1340, 1220, 1140.
Mass: m/z 331 [M+ ]
Starting Material: methyl [5-(3-methylsulfonylamino-2-thienyl) tetrazol-1-yl] acetate
M.P.: 154-155°C
N.M.R. (CDCl3) δppm: 3.01 (s, 3H); 3.78 (s, 3H); 5.38 (s, 2H); 7.53 (d, 1H, J=5.61 Hz); 7.62 (d, 1H, J=5.61 Hz); 9.92 (bs, 1H).
I.R. νKBr (cm-1): 3150. 3100, 1740, 1560, 1370, 1330, 1220, 1150, 760.
Mass: m/z 303 [M+ ]
Starting Material: methyl [5-(3-butylsulfonylamino-2-thienyl) tetrazol-1-yl] acetate
M.P.: 158-159°C (decomposition)
N.M.R. (CDCl3) δppm: 0.87 (t, 2H, J=7.32 Hz); 1.35∼1.44 (m, 2H); 1.75∼1.85 (m, 2H); 3.14 (t, 2H, J=7.95 Hz); 3.84 (s, 3H); 5.45 (s, 2H); 7.54 (d, 1H, J=5.49 Hz); 7.62 (d, 1H, J=5.49 Hz); 9.98 (bs, 1H).
I.R. νKBr (cm-1): 3100, 2950, 1750, 1560, 1370, 1220, 1150.
Mass: m/z 345 [M+ ]
Starting Material: methyl [5-(3-phenylsulfonylamino)-2-thienyl) tetrazol-1-yl] acetate
M.P.: 124-125°C
N.M.R. (CDCl3) δppm: 3.72 (s, 3H); 5.23 (s, 2H); 7.31∼7.17 (m, 5H); 7.53 (d, 1H, J=5.62 Hz); 7.58∼7.91 (m, 2H): 10.16 (bs, 1H).
I.R. νKBr (cm-1): 3120, 2950, 1750, 1560, 1520, 1430. 1380, 1240, 1160, 760, 580.
Mass: m/z 365 [M+ ]
Starting Material: methyl [5-(3-hydroxy-2-thienyl)tetrazol-1-yl] acetate
M.P.: 199-200°C (decomposition)
N.M.R. (CDCl3) δppm: 4.36 (bs, 1H); 5.38 (s, 2H); 6.87 (d, 1H, J=5.37 Hz); 7.45 (d, 1H, J=5.37 Hz); 10.23 (bs, 1H).
I.R. νKBr (cm-1): 3450, 2850, 1720, 1440, 1230, 1120, 1010, 750. Mass: m/z 226 [M+ ]
Starting Material: methyl [5-(2-methylsulfinyl-3-thienyl)-tetrazol-1-yl] acetate
M.P.: 144-145°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 3.08 (s, 3H): 5.15 (d, 1H, J=17.82 Hz); 5.30 (d, 1H, J=17.82 Hz); 7.34 (d, 1H, J=5.12 Hz); 7.81 (d, 1H, J=5.12 Hz).
I.R. νKBr (cm-1): 3100, 2900, 1700, 1570, 1420, 1300, 1260, 1220, 1000, 760.
Mass: m/z 272 [M+ ]
Starting Material: methyl [5-(2-methylsulfonyl-3-thienyl)-tetrazol-1-yl ] acetate
M.P.: 135-136°C
N.M.R. (CDCl3 +DMSO-d6) δppm: 3.32 (bs, 1H); 3.48 (s, 3H); 5.37 (s, 2H); 7.40 (d, 1H, J=5.13 Hz); 8.32 (d, 1H, J=5.13 Hz).
I.R. νKBr (cm-1): 3500, 3100, 3000, 1720, 1310, 1140, 950, 760.
Mass: m/z 288 [M+ ]
Starting Material: methyl [5-(3-methylcarbonylamino 2-thienyl)-tetrazol-1-yl] acetate
M.P.: 258°C (decomposition)
N.M.R. (DMSO-d6) δppm: 2.34 (bs, 1H); 5.17 (s, 2H); 7.02 (d, 1H, J=5.50 Hz); 7.59 (d, 1H, J=5.50 Hz); 11.01 (bs, 1H).
I.R. νKBr (cm-1): 3240, 3160, 1700, 1590, 1530, 1380, 1040, 770.
Starting Material: methyl [5- [5- [N-methyl-N- [2-(methoxyethoxy)-ethyl] aminosulfonyl]-2-thienyl] -tetrazol-1-yl] acetate
N.M.R. (CD3 OD) δppm: 2.77 (s, 3H); 3.07 (t, 2H, J=5.61 Hz); 3.60 (t, 2H, J=5.61 Hz); 5.24 (s, 2H); 7.26 (d, 1H, J=5.13 Hz); 8.02 (d, 1H, J=5.13 Hz).
I.R. νNaCl (cm-1): 3450, 2950, 1740, 1440, 1350, 1150, 1040, 590.
Mass: m/z 347 [M+ ]
PAC (3-1) methyl [5-(2-thienyl)tetrazol-1yl] acetateTo a solution of 500 mg (2.51 mM) of N-(2-thenoyl)glycine methyl ester in 5 ml of anhydrous methylene chloride, there were added, at room temperature, 185 mg (2.53 mM) of anhydrous N,N-dimethylformamide and 418 mg (3.51 mM) of thionyl chloride and then the mixture was refluxed for one hour. The reaction solution was concentrated at 40° c. under reduced pressure and the resulting residue was dissolved in 5 m l of anhydrous N,N-dimethylformamide.
The resulting solution was dropwise added to a suspension of 410 mg (6.3 mM) of sodium azide in 3 ml of anhydrous N,N dimethylformide at a temperature of the suspension ranging from 5° to 10°C over 30 minutes with stirring. After the dropwise addition, the reaction mixture was stirred for additional 30 minutes at room temperature, poured into ice-water and extracted with ethyl acetate. The organic phase obtained was washed with water, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant residue was recrystallized from ethyl acetate/n hexane to give 395 mg (yield 70.2%) of methyl [5-(2-thienyl)tetrazol-1-yl] acetate.
The results of the instrumental analysis of the product are consistent with those for the product obtained in Example (1-1).
To a solution of 1 g (4.69 mM) of N-(3-thenoyl)glycine methyl ester in 10 ml of anhydrous methylene chloride, there were added, at room temperature, 350 mg (4.79 mM) of anhydrous N,N-dimethylformamide and 800 mg (6.72 mM) of thionyl chloride and then the mixture was refluxed for one hour. The reaction solution was concentrated at 40°C under reduced pressure and the resulting residue was dissolved in 10 ml of anhydrous N,N-dimethylformamide.
the resulting solution was dropwise added to a suspension of 800 mg (12.3 mM) of sodium azide in 5 ml of anhydrous N,N-dimethylformamide as a temperature of the suspension ranging from 5° to 10°C over 30 minutes and stirring. After the dropwise addition, the reaction mixture was stirred for additional 30 minutes at room temperature, poured into ice-water and extracted with ethyl acetate. The organic phase obtained was washed with water, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant residue was recrystallized from ethyl acetate/n hexane to give 730 mg (yield 65.3%) of ethyl [5-(3-thienyl)tetrazol-1-yl] acetate.
M.P.: 69.5-70.5°C
N.M.R. (CDCl3) δppm: 1.27 (t, 3H, J=7.25 Hz); 4.26 (g, 2H, J=7.25 Hz); 5.25 (s, 2H); 7.48 (dd, 1H, J=5.20, 1.21 Hz); 7.55 (dd, 1H, J=5.20, 2.82 Hz); 7.84 (dd, 1H, J=2.82, 1.21 Hz).
I.R. νKbr (cm-1): 3100, 2970, 2950, 1740, 1570, 1440, 1370, 1210, 880.
Mass: m/z 238 [M+ ]
The following compounds were prepared in the same manner as described above.
Starting Material: N-(3-methoxy-2-thenoyl)glycine methyl ester
M.P.: 121-122°C
N.M.R. (CDCl3) δppm: 3.76 (s, 3H); 3.90 (s, 3H); 5.34 (s, 2H); 6.97 (d, 1H, J=5.64 Hz); 7.54 (d, 1H, J=5.64 Hz).
I.R. νKBr (cm-1): 3100, 2950, 1760, 1580, 1520, 1400, 1240, 1220, 1070, 760.
Mass: m/z 254 [M+ ]
Starting Material: N-(3-butoxy-2-thenoyl)glycine methyl ester
M.P.: 62-62.5°C
N.M.R. (CDCl3) δppm: 0.88 (t, 3H, J=7.26 Hz); 1.28∼1.39 (m, 2H); 1.59∼1.70 (m, 2H); 3.66 (s, 3H); 4.04 (t, 2H, J=6.85 Hz); 5.34 (s, 2H); 6.84 (d, 1H, J=5.64 Hz); 7.45 (d, 1H, J=5.64 Hz).
I.R. νKBr (cm-1); 3100, 2950, 1760, 1580, 1510, 1400, 1240, 1220, 1050, 750.
Mass: m/z 296 [M+ ]
Starting Material: N-(5-butyl-2-thenoyl)glycine methyl ester
M.P.: 58-59°C
N.M.R. (CDCl3) δppm: 0.95 (t, 3H, J=7.32 Hz); 1.37∼1.46 (m, 2H); 1.65∼1.76 (m, 2H); 2.88 (t, 2H, J=7.32 Hz); 3.83 (s, 3H); 5.32 (s, 2H); 6.89 (d, 1H, J=3.66 Hz); 7.38 (d, 1H, J=3.66 Hz).
I.R. νKBr (cm-1): 2950, 1740, 1580, 1520, 1440, 1380, 1220, 1100, 1000, 800.
Mass m/z 280 [M+ ]
Starting Material: N-(5-phenylpropyl-2-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 2.06 (quint., 2H, J=7.57 Hz); 2.71 (t, 2H, J=7.57 Hz); 2.91 (t, 2H, J=7.57 Hz); 3.83 (s, 3H); 5.31 (s, 2H); 6.90 (dt, 1H, J=3.72 0.73 Hz); 7.18∼7.34 (m, 5H); 7.40 (d, 1H, J=3.72 Hz).
I.R. νNaCl (cm-1): 2920, 1750, 1580. 1500, 1440, 1220, 1100, 700.
Mass: m/z 342 [M+ ]
Starting Material: N-(5-methoxymethyl-2-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 3.44 (s, 3H); 3.84 (s, 3H); 4.67 (d, 2H, J=0.73 Hz); 5.33 (s, 2H); 7.10 (dt, 1H, J=3.66, 0.73 Hz); 7.48 (d, 1H, J=3.66 Hz).
I.R. νNaCl (cm-1): 2950, 1750, 1580, 1440, 1360, 1220, 1000, 800.
Mass: m/z 268 [M+ ]
Starting Material: N-(5-butoxymethyl-2-thenoyl)glycine methyl ester
M.P.: 48-49°C
N.M.R. (CDCl3) δppm: 0.93 (t, 3H, J=7.21 Hz); 1.33∼1.45 (m, 2H); 1.56∼1.66 (m, 2H); 3.54 (t, 2H, J=6.74 Hz); 3.83 (s, 3H); 4.70 (d, 2H, J=0.73 Hz); 5.33 (s, 2H); 7.07 (dt, 1H, J=3.72, 0.73 Hz); 7.46 (d, 1H, J=3.72 Hz).
I.R. νKBr (cm-1): 2950, 2850, 1740, 1580, 1420, 1230, 1100, 800.
Mass: m/z 310 [M+ ]
Starting Material: N-(2-bromo-3-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 3.76 (s, 3H); 5.17 (s, 2H); 7.10 (d, 1H, J=5.73 Hz); 7.48 (d, 1H, J=5.73 Hz).
I.R. νNaCl (cm-1): 3100, 2950, 1750, 1580, 1430, 1220, 1000
Mass: m/z 303 [M+ ]
Starting Material: N- [2- (oct-4-yl)-3-thenoyl] glycine methyl ester
N.M.R. (CDCl3) δppm: 0.78∼0.85 (m, 6H); 1.11∼1.26 (m, 6H); 1.50∼1.67 (m, 4H); 3.12∼3.18 (m, 1H); 3.81 (s, 3H); 5.05 (s, 2H); 6.93 (d, 1H, J=5.37 Hz); 7.36 (d, 1H, J=5.37 Hz).
I.R. νNaCl (cm-1): 2950, 2850, 1760, 1440, 1220.
Mass: m/z 336 [M+ ]
Starting Material: N-)2-methylthio-3-thenoyl)glycine methyl ester
M.P. 90-91°C
N.M.R. (CDCl3) δppm: 2.47 (s, 3H); 3.75 (s, 3H); 5.20 (s, 2H); 7.15 (d, 1H, J=5.37 Hz); 7.46 (d, 1H, J=5.37 Hz).
I.R. νKBr (cm-1): 3110, 2920, 1750, 1550, 1420, 1220, 1100.
Mass: m/z 270 [M+ ]
Starting Material: N-(2-phenylthio-3-thenoyl)glycine methyl ester
N.M.R. (CDCl3) δppm: 3.73 (s, 3H); 5.10 (s, 2H); 7.21∼7.27 (M, 6H); 7.55 (d, 1H, J=5.37 Hz).
I.R. νNaCl (cm-1): 3100, 2950, 1750, 1570, 1480, 1440, 1360, 1220, 1000.
Mass: m/z 332 [M+ ]
Starting Material: N-(5-phenylthio-2-thenoyl)glycine methyl ester
M.P.: 102-103°C
N.M.R. (CDCl3) δppm: 3.82 (s, 3H); 5.30 (s, 2H); 7.26∼7.37 (m, 6H); 7.49 (d, 1H, J=3.91 Hz).
I.R. νKBr (cm-1): 2900, 1750, 1570, 1480, 1430, 1410, 1360, 1220, 1100, 800.
Mass: m/z 332 [M+ ]
Starting Material: N-[5-(N',N'-diethylaminosulfonyl)-2-thenoyl)-glycine methyl ester
N.M.R. (CDCl3) δppm: 1.08 (t, 6H; J=7.20 Hz); 3.07 (g, 4H, J=7.20 Hz); 3.72 (s, 3H); 5.23 (s, 2H); 7.22 (d, 1H, J=5.12 Hz); 7.67 (d, 1H, J=5.12 Hz).
I.R. νNaCl (cm-1): 3100, 2950, 1750, 1610, 1440, 1350, 1220, 1150, 940, 700.
Mass: m/z 347 [M+ ]
Starting Material: N- [5-(N',N'-dibutylaminosulfonyl)-2-thenoyl)-glycine methyl ester
N.M.R. (CDCl3) δppm: 0.86 (t, 6H, J=7.32 Hz); 1.33∼1.37 (m, 4H); 1.40∼1.48 (m, 4H); 2.04 (t, 4H, J=7.32 Hz); 3.71 (s, 3H); 5.23 (s, 2H); 7.22 (d, 1H, J=5.25 Hz); 7.67 (d, 1H, J=5.25 Hz).
I.R. νNaCl (cm-1): 2950, 1760, 1360, 1220, 1150.
Mass: m/z 415 [M+ ]
Starting Material: N-(5-piperidinosulfonyl-2-thenoyl)glycine methyl ester
M.P.: 133-135°C
N.M.R. (CDCl3) δppm: 1.04∼1.53 (m, 2H); 1.59∼1.68 (m, 4H); 2.92 (t, 4H, J=5.25 Hz); 3.71 (s, 3H); 5.23 (s, 2H); 7.26 (d, 1H, J=5.13 Hz); 7.72 (d, 1H, J=5.13 Hz).
I.R. νKBr (cm-1): 3100, 2950, 1760, 1340, 1220, 1150, 940, 710, 590.
Mass m/z 371 [M+ ](3-17) methyl [5- [2-(N,N-diethylaminosulfonyl)-5-trimethylsilyl-3-thienyl] tetrazol-1-yl] acetate; (yield=75.4%)
Starting Material: N- [2-(N',N'-diethylaminosulfonyl)-5-trimethylsilyl-3-thenoyl] glycine methyl ester
N.M.R. (CDCl3) δppm: 0.37 (s, 9H); 1.08 (t, 6H, J=7.20 Hz); 3.06 (g, 4H, J=7.08 Hz); 3.71 (s, 3H); 5.21 (s, 2H); 7.24 (s, 1H).
I.R. νNaCl (cm-): 2950, 1760, 1440, 1350, 1250, 1220, 1140, 1000, 840, 700.
Mass m/z 431 [M+ ]
Starting Material: N-(3-hydroxy-2 thenoyl)glycine methyl ester
M.P.=141-142°C
N.M.R. (CDCl3) δppm: 3.84 (s, 3H); 5.38 (s, 2H); 6.95 (d, 1H, J=5.37 Hz); 7.46 (d, 1H, J=5.37 Hz); 10.12 (bs, 1H).
I.R. νKBr (cm-1): 3100, 1760, 1740, 1530, 1220, 1000.
Mass: m/z 240 [M+ ]
The compounds prepared in the foregoing Examples are listed in the following Table I.
| TABLE I |
| ______________________________________ |
| Ex. |
| No. R1 R2 X |
| ______________________________________ |
| 1-1 --CH3 |
| H S (2)*2 |
| 1-2 --CH3 |
| --CH3 (3)*1 S (2) |
| 1-3 --CH3 |
| --CH3 (4) S (2) |
| 1-4 --CH3 |
| --CH3 (5) S (2) |
| 1-5 --CH3 |
| H S (3) |
| 1-6 --CH3 |
| H O (2) |
| 1-7 --CH3 |
| H O (3) |
| 1-8 --CH3 |
| --CH2 CH3 (5) S (2) |
| 1-9 --CH3 |
| --CH2 -on (5) S (2) |
| 1-10 --CH3 |
| --SCH3 5) S (2) |
| 1-11 --CH3 |
| --Br (5) S (2) |
| 1-12 --CH3 |
| --CH3 (2) S (2) |
| 1-13 --CH3 |
| --CH2 Br (5) S (2) |
| 1-14 --CH3 |
| on (5) |
| S (2) |
| 1-15 --CH3 |
| --NHCOCH3 (3) S (2) |
| 1-16 --CH3 |
| --NHCOCH2 CH2 CH3 (3) |
| S (2) |
| 1-17 --CH3 |
| --NHCOCH2 CH2 -on (3) |
| S (2) |
| 1-18 --CH3 |
| --CH3 (5) O (2) |
| 1-19 --CH3 |
| --CH2 CH2 CH2 CH3 (5) |
| O (2) |
| 1-20 --CH3 |
| --Br (5) O (2) |
| 1-21 --CH3 |
| --SCH3 (5) O (2) |
| 1-22 --CH3 |
| --Br (2) O (3) |
| 1-23 --CH3 |
| --CH(n-C3 H7)--CH2 CH2 CH2 CH3 |
| (2) O (3) |
| 1-24 --CH3 |
| --SCH3 (2) O (3) |
| 1-25 --CH3 |
| --NHSO2 CH3 (3) |
| S (2) |
| 1-26 --CH3 |
| --NHSO2 CH2 CH2 CH2 CH3 |
| S (2) |
| 1-27 --CH3 |
| --NHSO2 on (3) S (2) |
| 1-28 --CH3 |
| --CH3 (2) O (3) |
| 1-29 --CH3 |
| --SO2 N(CH3)--CH2 CH2 OCH2 OCH3 |
| (5) S (2) |
| 2-1 --H H S (2) |
| 2-2 --H --CH3 (3) S (2) |
| 2-3 --H --CH3 (4) S (2) |
| 2-4 --H --CH3 (5) S (2) |
| 2-5 --H H S (3) |
| 2-6 --H H O (2) |
| 2-7 --H H O (3) |
| 2-8 --H --C2 H5 (5) S (2) |
| 2-9 --H --CH2 -on (5) S (2) |
| 2-10 --H --SCH3 (5) S (2) |
| 2-11 --H --Br (5) S (2) |
| 2-12 --H --CH3 (2) S (3) |
| 2-13 --H --CH2 Br (5) S (2) |
| 2-14 --H |
| on (5) |
| S (2) |
| 2-15 --H --OCH3 (3) S (2) |
| 2-16 --H --OCH2 CH2 CH2 CH3 (3) |
| S (2) |
| 2-17 --H --NHCOCH3 (3) S (2) |
| 2-18 --H --NHCOCH2 CH2 CH3 (3) |
| S (2) |
| 2-19 --H --NHCOCH2 CH3 -on (3) |
| S (2) |
| 2-20 --H --CH2 CH2 CH2 CH3 (5) |
| S (2) |
| 2-21 --H --CH2 CH2 CH3 -on (5) |
| S (2) |
| 2-22 --H --CH2 OCH3 (5) |
| S (2) |
| 2-23 --H --CH2 OCH2 CH2 CH2 CH3 |
| S (2) |
| 2-24 --H --Br (2) S (3) |
| 2-25 --H --CH(n-C3 H7)--CH2 CH2 CH2 CH2 |
| (2) S (3) |
| 2-26 --H --SCH3 (2) S (3) |
| 2-27 --H --CH3 (5) O (2) |
| 2-28 --H --CH2 CH2 CH2 CH3 (5) |
| O (2) |
| 2-29 --H --Br (5) O (2) |
| 2-30 --H --SCH3 (5) O (2) |
| 2-31 --H --Br (2) O (3) |
| 2-32 --H --SCH3 (2) O (3) |
| 2-33 --H --S-on (2) S (3) |
| 2-34 --H --S-on (5) S (2) |
| 2-35 --H --SO2 --N(C2 N5)2 (5) |
| S (2) |
| 2-36 --H --SO2 --NCH2 CH2 CH2 CH3)2 |
| S (2) |
| 2-37 --H --SO2 -on (5) S (2) |
| 2-38 --H --SO2 --N(C2 H5)2 (2) |
| S (3) |
| 2-39 --H --NHSO2 CH3 (3) |
| S (2) |
| 2-40 --H --NHSO2 CH2 CH2 CH2 CH3 |
| S (2) |
| 2-41 --H --NHSO3 -on (3) S (2) |
| 2-42 --H --ON (3) S (2) |
| 2-43 --H --SOCH3 (2) S (3) |
| 2-44 --H --SO2 CH3 (2) S (3) |
| 2-45 --H --NH2 HCl (3) S (2) |
| 2-46 --H --SO2 --N(CH3)--CH2 CH2 OH |
| S (2) |
| 3-1 --CH3 |
| H S (2) |
| 3-2 --C2 H5 |
| H S (3) |
| 3-3 --CH3 |
| --OCH3 (3) S (2) |
| 3-4 --CH3 |
| --OCH2 CH2 CH2 CH3 (3) |
| S (2) |
| 3-5 --CH3 |
| --CH2 CH2 CH2 CH3 (5) |
| S (2) |
| 3-6 --CH3 |
| --CH2 CH2 CH2 -on (5) |
| S (2) |
| 3-7 --CH3 |
| --CH2 OCH3 (5) |
| S (2) |
| 3-8 --CH3 |
| --CH2 OCH2 CH2 CH2 CH3 |
| S (2) |
| 3-9 --CH3 |
| --Br (2) S (3) |
| 3-10 --CH3 |
| --CH(n-C3 H7)CH2 CH2 CH2 CH3 |
| (2) S (3) |
| 3-11 --CH3 |
| --SCH3 (2) S (3) |
| 3-12 --CH3 |
| --S-on (2) S (3) |
| 3-13 --CH3 |
| --S-on (5) S (2) |
| 3-14 --CH3 |
| --SO2 --N(C3 H5)2 (5) |
| S (2) |
| 3-15 --CH3 |
| --SO2 --N(n-C3 H5)2 (5) |
| S (2) |
| 3-16 --CH3 |
| --SO2 -on (5) S (2) |
| 3-17 --CH3 |
| --SO2 --N(C2 H5)2 (2) |
| S (3) |
| --Si(CH3)3 (%) |
| 3-18 H --OH (3) S (2) |
| ______________________________________ |
| In Table I on" and pip" means a phenyl and piperidine groups respectively |
| *1 Each numeral given in parentheses means the position on the |
| thiophene or furan ring at which each substituent is bonded. |
| *2 Each numeral given in parentheses means the position on the |
| thiophene or furan ring at which the tetrazolyl group is bonded at its |
| 5position. |
thiophene or furan ring at which the tetrazolyl group is bonded at its 5-position.
As has been explained above in detail, the aldose reductast inhibitor of the present invention shows excellent aldose reductase inhibitory effect and has low toxicity. Therefore, it can be used as a medicine for preventing and/or treating mammalian inclusive of man suffering from diabetic complications such as neural disorders, nephrosis, cataract and retinopathy with safety.
The effects and toxicity of the aldose reductase inhibitor according to the present invention will be detailed below with reference to the following Test Examples.
PAC (i) MethodologySix-weeks-old male SD rates were anesthetized with ether and killed. Then their crystalline lenses were immediately removed and stored at -80°C The lenses were homogenized in 3 volume of 135 mM sodium potassium phosphate buffer (pH 7.0) and centrifuged at 30,000 rpm for 30 minutes. the resulting supernatant was dialyzed overnight against 0.05 M sodium chloride solution to obtain an aldose reductase solution. All operations were conducted at 4°C and the enzyme solution was stored at -80°C
The activity of aldose reductase was determined according to a partially modified method of J.H. Kinoshita et al (J. Bio. Chem., 1965, 240, p. 877). More specifically, 0.1 ml of DL glyceraldehyde (final concentration: 10 mM) was added to 0.9 ml of 100 mM sodium potassium phosphate buffer (pH 6.2) which contained lithium sulfate (final concentration: 400 mM), reduced nicotinamide adenine dinucleotide phosphate (final concentration: 0.15 mM), the enzyme solution, and the compound to be evaluated (final concentration: 10-6 M, 10-7 M or 1031 8 M), and then the reaction was conducted at 30°C for 5 minutes. During the reaction, the change in the absorbance at 340 nm with time was monitored. The maximum reducing rate of the absorbance (U) during the reaction was determined. By subtracting, from this value, the maximum reducing rate (Uo) at 340 nm of the reaction solution before the addition of the substrate (DL-glyceraldehyde), the reaction rate (V=U-Uo) was calculated as a true reaction rate in the presence of the compound to be tested.
The same procedure was repeated except for the absence of the compound to be tested. A true reaction rate (Vo) in case the enzyme was not inhibited was calculated (Vo =U'-Uo '). The aldose reductase inhibitory activity of the test compounds was determined according to the following formula:
Rate of Inhibition (%)=(Vo -V)/Vo ×100
For comparison, the same tests were conducted using a known aldose reductase inhibitor: ONO-2235 [(E)-3-carboxymethyl-5- [(2E)-methyl-3-phenylpropenylidene] rhodan].
The results thus obtained are summarized in the following Table II. As seen from Table II, the compounds of the present invention tested show aldose reductase inhibitory effect identical to or superior to those attained by the known inhibitor ONO-2235.
| TABLE II |
| ______________________________________ |
| Compound Tested IC50 |
| (Ex. No.) (10-4) M |
| ______________________________________ |
| 1-5 96 |
| 1-7 74 |
| 1-27 23 |
| 2-1 1.6 |
| 2-2 1.8 |
| 2-3 2.4 |
| 2-4 2.3 |
| 2-5 2.1 |
| 2-6 6.0 |
| 2-7 3.0 |
| 2-8 2.1 |
| 2-9 2.0 |
| 2-10 2.0 |
| 2-11 1.9 |
| 2-12 1.0 |
| 2-13 2.5 |
| 2-14 2.1 |
| 2-15 2.9 |
| 2-16 3.1 |
| 2-17 2.8 |
| 2-18 2.0 |
| 2-19 2.4 |
| 2-20 2.3 |
| 2-21 2.8 |
| 2-22 3.1 |
| 2-23 2.5 |
| 2-24 3.8 |
| 2-26 3.1 |
| 2-27 15 |
| 2-28 13 |
| 2-29 16 |
| 2-30 11 |
| 2-31 8.5 |
| 2-32 3.5 |
| 2-33 2.4 |
| 2-34 2.6 |
| 2-35 39 |
| 2-36 8.5 |
| 2-37 23 |
| 2-38 46 |
| 2-39 2.8 |
| 2-40 1.6 |
| 2-41 2.3 |
| 2-42 2.0 |
| 2-43 30 |
| 2-44 52 |
| 3-2 58 |
| 3-5 18 |
| 3-11 38 |
| ONO-2235 2.2 |
| ______________________________________ |
Groups of 6 to 8-weeks-old Sprague-Dawley male rats (4 aminals per group) were fasted for 18 hours and streptozotocin was injected through the tail vein in a dose of 60 mg/kg to thus obtain diabetic rats. Immediately after the administration of the streptozotocin, each compound to be tested was orally administered to these rats in the form of a suspension at a dose of 10 mg/kg, 30 mg/kg and 50 mg/kg (each was suspended in a 0.5% sodium carboxymethyl cellulose solution) twice a day (9 o'clock in the morning and 5 o'clock in the afternoon) for 5 days. During the test, the rats took diet and drank water freely. 4 Hours after the final administration of the drug in the 5th day's morning (9 o'clock in the morning), the rats were sacrificed and then the sciatic nerve thereof was removed to determine the amount of sorbitol accumulated therein.
The results are expressed in the percentage obtained while the value obtained on the control to which any drug was not administered is defined to be 100.
The results of the test are listed in the following Table III. These results indicate that the compounds of the present invention shown high inhibitory effect as compared with those for the known aldose reductase inhibitor ONO-2235.
| TABLE III |
| ______________________________________ |
| Rate of Inhibition of |
| Compound Tested Sorbitol Accumulation (%) |
| (Ex. No.) 10 mg/kg 30 mg/kg 50 mg/kg |
| ______________________________________ |
| 2-1 68 89 -- |
| 2-2 62 93 -- |
| 2-5 73 90 -- |
| 2-7 46 77 -- |
| ONO-2235 0 0 40 |
| ______________________________________ |
Each compound to be tested was suspended to 0.5% sodium carboxymethyl cellulose solution and the resulting suspension was orally administered to 6-weeks-old male MCH mice (5 animals per test group). The 50% lethal dose (LD50 ; mg/kg) was evaluated from the mortality rate (%) observed 14 days after the administration of the compound. The mice took diet and drank water freely during the test.
The results obtaind are summarized in the following Table IV. As seen from Table IV, the compounds of the present invention which were subjected to the foregoing test show LD50 of not less than 3,000 mg/kg.
| TABLE IV |
| ______________________________________ |
| Compound Tested (Ex. No.) |
| LD50 (mg/kg) |
| ______________________________________ |
| 2-1 >3.000 |
| 2-2 >3.000 |
| 2-3 >3.000 |
| ______________________________________ |
Goto, Masayoshi, Inukai, Sinji, Agata, Mitsuzi, Horio, Yoshihiro, Ootake, Yasuhiro, Sawaki, Shohei, Umezawa, Manami
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 4886885, | Oct 28 1987 | Lilly Industries Limited | Compound containing tetrazolyl groups and their use for treating allergies and cardiovascular disease |
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