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Production manner null of kinoronkarubon

机译:罗祖·奇恩·曼恩·努鲁·基诺隆·卡鲁邦

摘要

PURPOSE: To industrially and advantageously produce a quinolonecarboxylic acid derivative useful as an antimicrobial agent by using a new specific quinolonecarboxylic acid derivative as a raw material or an intermediate. ;CONSTITUTION: The objective 1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3- methylaminopiperidino)-4-oxo-3-quinolinecarboxylic acid, expressed by formula II and useful as an antimicrobial agent is obtained simply by hydrolyzing a new compound expressed by formula I (R1 and R2 are H or alkyl; R1 and R2, together with N, form a 5- or 6-membered cyclic amine). This new compound expressed by formula I is obtained by reacting a new compound expressed by formula III (X1 and X2 are halogen) with 3-methylaminopiperidine or its hydrochloride and further reacting the resultant new compound expressed by formula IV with a compound expressed by formula V (X3 is alkali metal).;COPYRIGHT: (C)1994,JPO&Japio
机译:用途:通过使用新的特定喹诺酮羧酸衍生物作为原料或中间体,在工业上有利地生产可用作抗菌剂的喹诺酮羧酸衍生物。 ;组成:目标式1-环丙基-6-氟-1,4-二氢-8-甲氧基-7-(3-甲基氨基哌啶子基)-4-氧代-3-喹啉羧酸,用作抗微生物剂简单地通过水解由式I表示的新化合物获得(R 1 和R 2 是H或烷基; R 1 和R 2 与N一起形成5元或6元环胺。通过使由式III表示的新化合物(X 1 和X 2 是卤素)与3-甲基氨基哌啶或其盐酸盐反应,再得到式I表示的该新化合物。使所得的式Ⅳ表示的新化合物与式Ⅴ表示的化合物(X 3 为碱金属)反应。COPYRIGHT:(C)1994,JPO&Japio

著录项

  • 公开/公告号JP3256325B2

    专利类型

  • 公开/公告日2002-02-12

    原文格式PDF

  • 申请/专利权人 中外製薬株式会社;

    申请/专利号JP19930092702

  • 发明设计人 藤村 保夫;三浦 裕;清水 裕仁;

    申请日1993-04-20

  • 分类号C07D401/04;C07D215/56;

  • 国家 JP

  • 入库时间 2022-08-22 01:00:11

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