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BRS-3 AGONISTS NOT PEPTIDIC.

机译:BRS-3激动剂不流行。

摘要

Compounds of the general formula I, ** see formula ** in which they mean A1 CH or, with the proviso that A2 does not represent a bond and A3, simultaneously, means NH, also nitrogen; A2 a bond, C1-2 alkylene or, with the proviso that A1 represents CH and R2 means hydrogen, also carbonyl; A3 methylene, optionally substituted with C1-4 alkyl or C1-4 alkylcarbonylamide or, with the proviso that R2 means hydrogen or together with R1 represents a bond, also NH; R1 hydrogen or, with the proviso that A2 represents carbonyl, also amino, and R2 hydrogen, or R1 and R2 together represent a bond, provided that A2 means a bond; R3 hydrogen or methyl; Ar1 phenyl, optionally substituted 1 to 2 times with halogen or C1-4alkyl, or with C1-2 alkylene-dioxy bonded to two adjacent ring carbon atoms, pyridyl, furyl, indolyl or tetrahydro-isoquinolyl; Ar2 furyl, benzofuranyl, thienyl, benzothiophenyl, pyrrolyl or indolyl; Ar3 phenyl, optionally substituted 1 to 2 times with halogen, or pyridyl; m 0 or 1, and n 0 or 1, as well as, if necessary, their salts by the addition of physiologically acceptable acid.
机译:通式Ⅰ的化合物,**参见式**,其中的化合物表示A1 CH或A2不代表键且A3同时表示NH和氮; A2是一个键,C1-2是亚烷基,或条件是A1代表CH,R2是氢,也是羰基; A3亚甲基,任选地被C1-4烷基或C1-4烷基羰基酰胺取代,或条件是R2是氢或与R1一起代表一个键,也是NH; R1为氢,或以A2为羰基,也为氨基,R2为氢,或R1和R2共同为键,条件是A2为键; R3为氢或甲基; Ar 1苯基,任选被卤素或C 1-4烷基或与结合在两个相邻的环碳原子上的C 1-2亚烷基-二氧基,吡啶基,呋喃基,吲哚基或四氢-异喹啉基取代1-2次的Ar 1苯基; Ar 2呋喃基,苯并呋喃基,噻吩基,苯并噻吩基,吡咯基或吲哚基; Ar 3苯基,任选地被卤素或吡啶基取代1-2次; m 0或1,n 0或1,以及必要时通过加入生理上可接受的酸形成其盐。

著录项

  • 公开/公告号ES2324709T3

    专利类型

  • 公开/公告日2009-08-13

    原文格式PDF

  • 申请/专利权人 SOLVAY PHARMACEUTICALS GMBH;

    申请/专利号ES20030757007T

  • 申请日2003-05-30

  • 分类号C07D209/20;A61K31/4045;A61K31/405;A61K31/4439;A61K38;A61K38/05;A61K38/06;A61P1/14;A61P3/04;A61P3/10;A61P9;A61P9/02;C07D401/12;C07D405/12;C07K5/06;C07K5/062;C07K5/065;C07K5/072;C07K5/078;C07K5/087;

  • 国家 ES

  • 入库时间 2022-08-21 19:23:43

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