首页> 外国专利> N- (HETEROCYCLYL) BENZENE OR PYRIDINE SULFONAMIDES AS ANTITROMBOSE AGENTS AND ANTICOAGULANTS

N- (HETEROCYCLYL) BENZENE OR PYRIDINE SULFONAMIDES AS ANTITROMBOSE AGENTS AND ANTICOAGULANTS

机译:N-(杂环基)苯或吡啶磺酰胺类作为抗凝血剂和抗癌剂

摘要

The invention relates to compounds of the formula wherein W may represent - (CH 2) 2 -, - (CH 2) -C C- or -CH 2 -CH = CH- group, R 2 may in particular denote a piperidinyl group, , 2,3,6-tetrahydropyridinyl group, optionally substituted hexahydro-1 (OH) -azepinyl group, piperazinyl group, optionally substituted or morpholinyl group, R 3 may denote a -COOR 1 group , A may in particular be a phenyl group, optionally substituted, a heterocycle or a cyclopentyl group, and B may in particular denote a pyridyl group, an aminopyrazinyl group, and a pyrimidinyl group optionally substituted by an amino group, a piperidinyl or aminopyridinyl group optionally substituted on pyridine by a (C 1 -C 4) alkyl or a (C 1 -C 4) alkoxy group, the amino group being optionally substituted by (C 1 -C 4) C1-C4) alkyl group. The invention also relates to the preparation of these compounds and to their therapeutic use.
机译:本发明涉及下式的化合物,其中W可以代表-(CH 2)2-,-(CH 2)-C C-或-CH 2 -CH = CH-基,R 2可以特别地表示哌啶基, ,2,3,6-四氢吡啶基,任选取代的六氢-1(OH)-a庚基,哌嗪基,任选取代或吗啉基,R 3可以表示-COOR 1基,A可以特别是苯基,任选地被取代的杂环或环戊基,并且B特别地表示吡啶基,氨基吡嗪基和嘧啶基,其任选地被氨基,哌啶基或氨基吡啶基任选地在吡啶上被(C 1- C 4)烷基或(C 1 -C 4)烷氧基,氨基任选被(C 1 -C 4)C 1 -C 4)烷基取代。本发明还涉及这些化合物的制备及其治疗用途。

著录项

  • 公开/公告号BG65863B1

    专利类型

  • 公开/公告日2010-03-31

    原文格式PDF

  • 申请/专利权人 SANOFI - SYNTHELABO;

    申请/专利号BG20020107130

  • 申请日2002-09-20

  • 分类号C07D211/70;C07D401/14;A61K;A61K31/195;A61K31/381;A61K31/44;A61K31/4427;A61K31/4436;A61K31/444;A61K31/445;A61K31/4545;A61K31/496;A61K31/497;A61K31/506;A61K31/5377;A61K31/55;A61P;A61P7/02;A61P43;C07D;C07D211/80;C07D213/73;C07D401/06;C07D401/12;C07D409/12;C07D409/14;

  • 国家 BG

  • 入库时间 2022-08-21 18:47:29

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