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1.6 - naphthyridin - 2 (1h) regions, procedure for their production and intermediates for use in

机译:1.6-萘啶-2(1h)区,其生产程序和用于

摘要

Naphthyridin-2(1 H)-ones, having the formula I …CHEM… or salts thereof, where Z is hydrogen or cyano, and Q is 2 (or 3)-furanyl, 2(or 3)-thienyl, 4(or 3)-pyridinyl or 4(or 3)-pyridinyl having one or two methyl substituents, are useful as cardiotonic agents and corresponding compounds where Z is carboxy are useful as intermediates. Also shown as intermediates are 5-(Q-CO)-6-[2(di-lower-alkylamino)-ethenyl]-2(1H)-pyridinones (II) or salts thereof, where Q is defined as above. A process for preparing the compounds (I) comprises reacting a compound (II) with formamidine, ammonia or a salt thereof.
机译:具有式I……的萘啶-2(1 H)-或其盐,其中Z为氢或氰基,Q为2(或3)-呋喃基,2(或3)-噻吩基,4具有一个或两个甲基取代基的(或3)-吡啶基或4(或3)-吡啶基可用作强心剂,而Z为羧基的相应化合物可用作中间体。还显示为中间体的是5-(Q-CO)-6- [2(二-低级烷基氨基)-乙烯基] -2(1H)-吡啶酮(II)或其盐,其中Q如上定义。制备化合物(I)的方法包括使化合物(II)与甲am,氨或其盐反应。

著录项

  • 公开/公告号DK13786D0

    专利类型

  • 公开/公告日1986-01-13

    原文格式PDF

  • 申请/专利权人 STERLING DRUG INC.;

    申请/专利号DK19860000137

  • 发明设计人 LESHER GEORGE YOHE;SINGH BALDEV;

    申请日1986-01-13

  • 分类号C07D;

  • 国家 DK

  • 入库时间 2022-08-22 07:42:25

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