首页> 外国专利> Benzodiazepine derivatives useful as metabotropic glutamate receptors

Benzodiazepine derivatives useful as metabotropic glutamate receptors

机译:苯二氮卓衍生物可用作代谢型谷氨酸受体

摘要

A benzodiazepine derivative or a pharmaceutically acceptable acid addition salt has the formula (I) wherein: X is a single bond or ethynediyl; when X is a single bond R1 is hydrogen, halogen, nitro, alkyl , haloalkyl, alkoxycarbonyl, optionally oxygen substituted cycloalkyl, optionally substituted benzoyl or phenyl, styrenyl, phenylethyl, naphthyl, biphenyl, benzofuranyl, or optionally substituted 5 or 6 membered heterocyclic ring; when X is ethynediyl R1 is hydrogen, optionally hydroxy substituted alkyl, haloalkyl, optionally substituted cycloalkyl or cycloalkenyl, alkenyl, optionally substituted phenyl, optionally substituted 5 or 6 membered heterocyclic ring or benzofuranyl; R3 is optionally substituted phenyl, pyridine, thiophenyl or thiazolyl; with the proviso when X is a single bond and R3 is pyridinyl, R1 is not hydrogen or methyl.
机译:苯并二氮杂卓衍生物或药学上可接受的酸加成盐具有式(I),其中:X为单键或乙炔二基;当X为单键时,R1为氢,卤素,硝基,烷基,卤代烷基,烷氧羰基,可选地被氧取代的环烷基,可选地被取代的苯甲酰基或苯基,苯乙烯基,苯乙基,萘基,联苯,苯并呋喃基或可选地被取代的5或6元杂环;当X为乙二基时,R1为氢,任选地为羟基取代的烷基,卤代烷基,任选地取代的环烷基或环烯基,烯基,任选地取代的苯基,任选地取代的5或6元杂环或苯并呋喃基; R3是任选取代的苯基,吡啶,噻吩基或噻唑基;当X是单键且R3是吡啶基时,R1不是氢或甲基。

著录项

  • 公开/公告号NZ518037A

    专利类型

  • 公开/公告日2004-04-30

    原文格式PDF

  • 申请/专利权人 F;

    申请/专利号NZ20000518037

  • 申请日2000-09-29

  • 分类号C07D243/12;A61K31/55;C07D409/04;C07D405/04;C07D417/04;C07D401/04;C07D403/10;C07D401/14;C07D417/14;C07D413/10;C07D405/06;C07D401/06;C07D417/10;C07F7/10;

  • 国家 NZ

  • 入库时间 2022-08-21 23:09:21

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号