首页> 外国专利> Preparation method of naftiridona or quinolone carboxylic acid derivatives substituted in position 7 by azacicloamina acid by coupling with a 7 - halogenorespectivo SAIn addition azacicloamina acid compound, compounds are antibacterial.

Preparation method of naftiridona or quinolone carboxylic acid derivatives substituted in position 7 by azacicloamina acid by coupling with a 7 - halogenorespectivo SAIn addition azacicloamina acid compound, compounds are antibacterial.

机译:通过与7-卤素视黄醛SA偶合,在7位被氮杂阿米巴胺酸取代的萘啶酮或喹诺酮羧酸衍生物的制备方法。此外,氮杂阿米巴胺酸化合物还具有抗菌作用。

摘要

Procedimientopara quinolone carboxylic acids and preparation of carboxylic acids naftindona antibacterial formual III, which has an external amino Group attached to their Substituent 7Without the use of blocking groups and subsequent Elimination in the external amino Group, which consists in contacting a compound of formula IV with a compound of formula (CH2) anh2 HR1.(g) B. In a Preferred embodiment, the naftiridona carboxylic acid is the trovafloxacina antibiotic.
机译:程序二对羟基喹诺酮羧酸和萘芬多纳羧酸盐形式的羧甲基纤维素的制备,其在取代基7上连接了一个外部氨基,而没有使用保护基,随后在外部氨基中进行了消除,这包括使式IV的一种化合物与一种在一个优选的实施方案中,萘啶酮羧酸是曲风沙星抗生素。

著录项

  • 公开/公告号CL1999001692A1

    专利类型

  • 公开/公告日2000-03-06

    原文格式PDF

  • 申请/专利权人 PFIZER PRODUCTS INC.;

    申请/专利号CL1999001692

  • 发明设计人 TIMOTHY NORRIS;

    申请日1999-07-26

  • 分类号A61K31/435;A61K31/47;C07D221/00;C07D401/04;C07D471/04;

  • 国家 CL

  • 入库时间 2022-08-22 01:57:00

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