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One Step procedure for the manufacture of 3 - quinoloncarboxilico acid derivatives

机译:一步法制备3-喹诺酮羧酸衍生物

摘要

Understand: 1) characterized by reacting an Acid Halide formula XXVI where Hal, x2 and X3 are f or CL, with: (a) a dimetilaminoacrilico acid ester of formula (CH3) 2n - ch = CH - coor,Followed by the addition of an Amine R1 - NH2; or (b) a aminoacrilester formula r1nh - ch = CH - coor; R is Methyl, Ethyl or propyl; 2) Heat (1) at a temperature of 60 degrees to 100 degrees.In a Solvent such as n-methyl pyrrolidone with POTASSIUM CARBONATE as an Auxiliary base, forming a nitrogen cycle; 3) reacting a Heterocyclic Compound with (2) ` r "N, rForming a compound of formula I, where r, R 'n Form "together with a Monkey or bicyclic heterocycle; is CH, CF, CCL, C - C - OCH3, CH3; x1 is H, halogen, CH3, NH2, R1 is alkyl fch2ch2 C1 - C3 -Ciclopropilo can be replaced by one to three halogens; which is useful as antibacterial
机译:理解:1)其特征在于,使卤代结构式XXVI(其中Hal,x2和X3为f或CL)与(a)通式为(CH3)的二甲氨基me啶酸酯2n-ch = CH-coor胺R1-NH2;或(b)氨基丙烯酸酯分子式r1nh-ch = CH-coor;或R为甲基,乙基或丙基; 2)在60至100度的温度下加热(1)。在溶剂中,例如以碳酸钾为辅助碱的正甲基吡咯烷酮,形成氮循环; 3)使杂环化合物与(2)`r “ N反应,形成式I化合物,其中r,R'n与猴子或双环杂环一起形成;是CH,CF,CCL,C-C-OCH3,CH3; x1是H,卤素,CH3,NH2,R1是烷基fch2ch2 C1-C3-环丙氟可被1-3个卤素取代;可用作抗菌剂

著录项

  • 公开/公告号PE33795A1

    专利类型

  • 公开/公告日1995-12-15

    原文格式PDF

  • 申请/专利权人 BAYER AKTIENGESELLSCHAFT;

    申请/专利号PE19940256625

  • 申请日1994-12-07

  • 分类号C07D215/233;C07D401/04;A61K31/47;A61K31/4709;C07D215/20;C07D215/56;C07D471/04;C07D498/04;C07D519;

  • 国家 PE

  • 入库时间 2022-08-22 03:53:01

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