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公开(公告)号:EP0040639A4
公开(公告)日:1982-03-22
申请号:EP80902298
申请日:1980-11-25
IPC分类号: A61K31/415 , A61K31/42 , A61K31/445 , A61K31/495 , A61K31/496 , A61K31/505 , A61K31/535 , A61K31/5377 , A61P1/08 , A61P25/00 , A61P25/04 , A61P25/26 , A61P29/00 , C07D261/04 , C07D413/04 , C07D413/06 , C07D413/14 , C07D471/04 , C07D471/10 , C07D471/20
CPC分类号: C07D471/04 , C07D261/04 , C07D471/10
摘要: Isoxazole derivatives represented by the following general formula: (FORMULA) (wherein Ar represents a phenyl or pyridyl group optionally substituted by halogen or lower alkoxy, R1 represents a hydrogen atom, a lower alkyl group or a group of Ar, R2 represents a hydrogen atom or, when R1 and R2 are taken together, they form a carbon-to-carbon bond, and Am represents an amine residue selected from the following: (FORMULA) wherein R3 represents a hydrogen atom or a lower alkyl group, X1 and X2 each represent a hydrogen atom, a halogen atom or a trifluoromethyl group, and Y represents 0 or S) and the salts thereof. These are useful as psychotropic drugs and antimetics.
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公开(公告)号:EP0125315A4
公开(公告)日:1985-06-26
申请号:EP83903564
申请日:1983-11-09
发明人: MURO TOMIO , TSUDA YOSHINAO , MISHINA TADASHI , OBATA MINORU , INUI JUN
IPC分类号: A61K31/425 , A61K31/426 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4412 , A61K31/445 , A61K31/505 , A61P9/06 , A61P9/08 , A61P9/10 , A61P9/12 , A61P25/02 , C07D213/64 , C07D213/65 , C07D213/68 , C07D239/34 , C07D277/20 , C07D277/34
CPC分类号: C07D213/64 , C07D213/65 , C07D213/68 , C07D239/34 , C07D277/34
摘要: Phenoxyaminopropanol derivatives represented by the general formula (I), wherein R represents 2-, 3- or 4-pyridyl, 2-pyrimidyl, 2-thiazolyl or 5-bromo-2-thiazolyl, R1 and R2 each represents H, lower alkyl, cycloalkyl, aralkyl or, when bound to each other, R1 and R2 represent a group forming a pyrrolidine or piperidine ring together with the adjacent nitrogen atom, and A represents alkylen containing 2 or 3 carbon atoms, and salts thereof. These are useful as heart-selective beta-blockers.
摘要翻译: 其中R表示2-,3-或4-吡啶基,2-嘧啶基,2-噻唑基或5-溴-2-噻唑基的通式(I)代表的苯氧基氨基丙醇衍生物,R1和R2各代表H,低级烷基, 环烷基,芳烷基或当彼此连接时,R1和R2代表与相邻的氮原子一起形成吡咯烷或哌啶环的基团,A代表含有2或3个碳原子的亚烷基及其盐。 这些作为心脏选择性β受体阻滞剂是有用的。
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