首页> 外国专利> method for preparing a medicine with bactericidal effect that a derivative of 3 - carboxy - dihydrochinolon - 4 contains.product obtained by this method and process for the preparation of these compounds.

method for preparing a medicine with bactericidal effect that a derivative of 3 - carboxy - dihydrochinolon - 4 contains.product obtained by this method and process for the preparation of these compounds.

机译:一种具有杀菌作用的药物的制备方法,其中3-羧基-二氢喹诺酮-4的衍生物含有通过该方法获得的产物以及制备这些化合物的方法。

摘要

1365839 Cyclopentenoquinoline derivatives BOEHRINGER MANNHEIM GmbH 3 May 1973 [10 May 1972] 21096/73 Heading C2C Novel compounds of Formula I (in which each of R and X is H or saturated or unsaturated, aliphatic C 1-5 hydrocarbyl, Y is OH, C 1-5 alkoxy or C 1-5 acyloxy and Z is H or C 1-5 alkoxy, or Y and Z together represent oxo or C 1-5 alkylenedioxy) and pharmacologically compatible salts thereof, are prepared by cyclizing a compound of the Formula II If desired, the product obtained may be N- alkylated, N-alkenylated or N-alkynylated and/ or rearranged, esterified, ketalized, reduced, oxidized, etherified or acylated to convert it to a different compound I, or it may be converted to a pharmacologically compatible salt. Pharmaceutical compositions having antimicrobial activity comprise a compound I, or a pharmacologically compatible salt thereof, together with a solid or liquid pharmaceutical carrier.
机译:1365839环戊烯喹啉衍生物BOEHRINGER MANNHEIM GmbH 1973年5月3日[1972年5月10日]标题C2C新型的式I化合物(其中R和X均为H或饱和或不饱和的脂族C 1-5烃基,Y为OH, C 1-5烷氧基或C 1-5烷氧基,Z为H或C 1-5烷氧基,或Y和Z一起代表oxo或C 1-5亚烷基二氧基)及其药理学上相容的盐,是通过将式II如果需要,所得产物可以被N-烷基化,N-烯基化或N-炔基化和/或重排,酯化,缩酮化,还原,氧化,醚化或酰化以将其转化为不同的化合物I,或者可以是转化为药理学上相容的盐。具有抗微生物活性的药物组合物包含化合物I或其药理学上相容的盐以及固体或液体药物载体。

著录项

  • 公开/公告号NL7306227A

    专利类型

  • 公开/公告日1973-11-13

    原文格式PDF

  • 申请/专利权人

    申请/专利号NL19730006227

  • 发明设计人

    申请日1973-05-04

  • 分类号C07D39/00;A61K27/00;

  • 国家 NL

  • 入库时间 2022-08-23 06:09:21

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