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derivatives of quinazoline derivatives of quinoleine and process for their preparation, and pharmaceutical compositions containing them

机译:喹唑啉衍生物的喹唑啉衍生物及其制备方法,以及含有它们的药物组合物

摘要

Compounds of formula I,whereinR1 represents C1-4 alkoxy optionally substituted by one or more fluorine atoms;R2 represents H or C1-4 alkoxy optionally substituted by one or more fluorine atoms;R3 represents a 5- or 6-membered heterocyclic ring, the ring being optionally substituted;R4 represents a 4-, 5-, 6-, or 7-membered heterocyclic ring, the ring being optionally fused to a benzene ring or a 5- or 6-membered heterocyclic ring, the ring system as a whole being optionally substituted;X represents CH or N; andL is absent, or represents a cyclic group of formula Ia, or represents a chain of formula Ib,and pharmaceutically acceptable salts thereof; are useful in therapy, in particular in the treatment of benign prostatic hyperplasia.
机译:式I的化合物,其中R 1代表任选地被一个或多个氟原子取代的C 1-4烷氧基; R 2代表任选地被一个或多个氟原子取代的H或C 1-4烷氧基; R 3代表5或6元杂环,环被任选地取代; R 4代表4、5、6或7元杂环,该环任选地稠合至苯环或5或6元杂环,整个环系统任选地被取代; X代表CH或N;和L不存在,或代表式Ia的环状基团,或代表式Ib的链,及其药学上可接受的盐;可用于治疗,特别是良性前列腺增生的治疗。

著录项

  • 公开/公告号MA26465A1

    专利类型

  • 公开/公告日2004-12-20

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号MA19980024920

  • 发明设计人 DAVID NATHAN ABRAHAM FOX;

    申请日1998-01-07

  • 分类号C07D215/12;C07D471/04;A61K31/47;A61K31/505;

  • 国家 MA

  • 入库时间 2022-08-21 22:17:35

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