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公开(公告)号:JPH03275679A
公开(公告)日:1991-12-06
申请号:JP7617390
申请日:1990-03-26
发明人: IWATA MICHIZOU , IMANISHI TAKESHI , SATO MASAKAZU , KAWASHIMA YUTAKA , GOTO JUN , CHIBA YOSHIYUKI , SATAKE MIKIO
IPC分类号: C07D277/04 , A61K31/425 , A61K31/426 , A61P7/02 , A61P9/08 , A61P9/10 , A61P11/08 , A61P25/28
摘要: NEW MATERIAL:A compound expressed by formula I [R is H, benzoyl or (substituted) phenyl sulfonyl; n is 0-3; X is H, halogen or lower alkoxy; R is expressed by formula II (R is H or lower alkyl) or expressed by formula III]. EXAMPLE:Ethyl 4-[(thiazolidine-2-yl)methyl]phenoxy acetate. USE:Used as an antagonist against thromboxane A2. Said compound has low toxicity and is useful for remedy of cerebrovascular twitch after subarachnoid hemorrhage and following cerebral ischemia symptom or asthma, etc. PREPARATION:An alcoholic substance expressed by formula IV is made to an aldehyde substance expressed by formula V by chromate oxidation with chromate anhydride, etc. Then, the aldehyde substance is reacted with cisthiamine hydrochloride in a solvent such as water or water-containing methanol to afford the compound expressed by formula I having H as the group R .
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公开(公告)号:JPH0373546B2
公开(公告)日:1991-11-22
申请号:JP1135683
申请日:1983-01-28
申请人: UBE INDUSTRIES
发明人: IWATA FUMIO , HARADA KATSUMASA , SUGISE RYOJI
IPC分类号: C07D277/04 , C07D277/10 , C07D279/06 , C07D281/02 , C07D283/02
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公开(公告)号:JPH03500886A
公开(公告)日:1991-02-28
申请号:JP50011789
申请日:1988-10-11
IPC分类号: C07D277/04 , A61K31/40 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4418 , A61K38/00 , A61P9/12 , C07C235/04 , C07C237/04 , C07C237/22 , C07C255/59 , C07C323/52 , C07C323/60 , C07D207/09 , C07D213/75 , C07D263/06 , C07D265/06 , C07K5/02 , C07K5/06 , C07K14/81
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公开(公告)号:JPH01301671A
公开(公告)日:1989-12-05
申请号:JP13224388
申请日:1988-05-30
申请人: SUNTORY LTD
IPC分类号: C12N9/99 , A61K31/425 , A61K31/426 , A61P25/28 , A61P43/00 , C07D277/04 , C07D277/06 , C07D417/06
摘要: NEW MATERIAL:A thiazolidine derivative shown I [n is 2 or 3; X is S, CH2 or CH(OH); R is nonsubstituted, substituted phenyl or 5-20C which may contain unsaturated bond; Y is O, CO or CH2]. EXAMPLE:N-(4-Phenylbutanoyl)proline-thiazolidinamide. USE:A drug having excellent anti-prolylendopeptidase activity extremely useful as a drug for alleviating amnesia. PREPARATION:A compound shown by formula II is condensed with a compound shown by formula III (R' is methyl or ethyl) in a solvent not to participate in the reaction in the presence of a condensation reagent to give a compound shown by formula IV. Then this compound is hydrolyzed with an alkali by a conventional procedure to give a carboxylic acid, which is condensed again with thiazolidine in a solvent not to participate in the reaction in the presence of a condensation agent to give a compound shown by formula I.
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公开(公告)号:JPH01199941A
公开(公告)日:1989-08-11
申请号:JP31363588
申请日:1988-12-12
申请人: BASF AG
IPC分类号: C07D277/04 , C07C319/02 , C07C319/06 , C07C323/25 , C07C323/58 , C07D277/60
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公开(公告)号:JPS646263A
公开(公告)日:1989-01-10
申请号:JP3867588
申请日:1988-02-23
发明人: TODA MASAAKI , OUCHIDA SHUICHI , ONO HIROYUKI
IPC分类号: C12N9/99 , A61K31/425 , A61K31/426 , A61K31/445 , A61K31/47 , A61K31/505 , A61P25/28 , A61P43/00 , C07D277/04 , C07D277/06 , C07D417/06
摘要: NEW MATERIAL:The thiazolidine derivative of formula I [R is G-E-D-B-A-; A and B are single bond or 1-6C alkylene, A may be 2-6C alkenylene or group of formula II-III; Y is 1-4C alkylene or 2-4C alkenylene; D is single bond, O, CO or group of formula IV-V; R is H, 1-4C alkyl, phenyl or benzyl; E is single bond or 1-8C alkylene which may have substituent (phenyl or ben zyl); G is carbon ring or heterocyclic group which may have 1-3 substituents (1-6C alkyl, halogen, CF3 or NO2); A and B are not single bond at the same time]. EXAMPLE:4(R)-3-[3-[N-(4-methylbenzyl)carbamoyl]propionyl]thiazolidin-4 -al. USE:A prolylendopeptitase inhibitor useful as an antiamnestic agent. PREPARATION:The compound of formula I can be produced by oxidizing a compound of formula VI [R is G-E-D -B-A-; D is D or CH(OH)] under mild condition.
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公开(公告)号:JPS63277642A
公开(公告)日:1988-11-15
申请号:JP8802988
申请日:1988-04-08
申请人: LILLY CO ELI
IPC分类号: C07D277/04 , A61K31/12 , A61K31/19 , A61K31/215 , A61K31/275 , A61K31/38 , A61K31/382 , A61K31/41 , A61K31/425 , A61K31/426 , A61K31/433 , A61P11/00 , A61P37/08 , A61P43/00 , C07C49/00 , C07C51/00 , C07C51/08 , C07C51/347 , C07C53/132 , C07C59/125 , C07C59/64 , C07C59/90 , C07C67/00 , C07C69/732 , C07C69/738 , C07C201/00 , C07C205/45 , C07C213/00 , C07C225/22 , C07C229/42 , C07C229/44 , C07C253/00 , C07C255/15 , C07C255/33 , C07C257/04 , C07C313/00 , C07C317/24 , C07C317/28 , C07C317/44 , C07C317/46 , C07C317/48 , C07C323/18 , C07C323/19 , C07C323/22 , C07C323/29 , C07C323/62 , C07D257/04 , C07D285/10 , C07D335/00 , C07D417/04
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公开(公告)号:JPS6354712B2
公开(公告)日:1988-10-28
申请号:JP15813079
申请日:1979-12-07
申请人: SOGO YATSUKO KK
发明人: OOSAWA YASUKO , UCHIKUGA SABURO
IPC分类号: C07D277/04 , C07D277/60
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公开(公告)号:JPS63203672A
公开(公告)日:1988-08-23
申请号:JP3570587
申请日:1987-02-20
申请人: KOWA CO
IPC分类号: C07D513/04 , A61K31/425 , A61K31/426 , A61K31/428 , A61K31/44 , A61K31/495 , A61K31/535 , A61P1/04 , A61P1/16 , C07D277/04 , C07D277/18 , C07D277/20 , C07D277/38 , C07D277/40 , C07D277/42 , C07D277/44 , C07D277/50 , C07D277/82 , C07D417/06 , C07D417/12
摘要: NEW MATERIAL:The compound of formula I {R1 and R2 are H, alkyl, alkoxy, phenyl, etc., or together form group of formula II (R3 is alkyl, alkoxy, acyl, phenyl, etc.; n is 0-4); A is group of formula III or formula IV [R4-R7 are H, CN or B-R8 (B is Alk, CO, Alk-CO, SO2, Alk-SO2, etc.; Al is alkylene or alkenylene; R8 is H, halogen, amino, aryl, etc.)]}. EXAMPLE:3-Methyl-2-cyanoiminobenzothiazoline. USE:An antiulcer agent and a remedy for hepatopathy. PREPARATION:For example, a compound of formula VII can be produced by reacting a compound of formula V with a dimethyl cyanamidothiocarbonate of formula VI.
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公开(公告)号:JPS6330901B2
公开(公告)日:1988-06-21
申请号:JP14882279
申请日:1979-11-19
IPC分类号: C07D295/02 , A61K31/415 , A61K31/445 , A61K31/495 , A61P31/12 , A61P35/00 , A61P43/00 , C07D231/12 , C07D233/58 , C07D277/04 , C07D295/03 , C07D521/00
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