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Sefuarosuhorinjudotaioyobisonoen

机译:塞夫·阿罗斯·霍林朱德腰带及其圈子

摘要

NEW MATERIAL:A compound shown by the formula I (R1 is lower alkyl; R2 is H, or lower alkyl; Y is 5- - 6-membered heterocyclic ring; n is 0-2) and its salt. EXAMPLE:7beta-[2-( 2-Aminothiazol-4-yl )-2-methoxyiminoacetamido]-3-[4-(imidazol-1- yl)pyridinio]methyl-3-cephem-4-carboxylate.trihydrochloride(syn-isomer). USE:An antibacterial agent against Gram-positive and Gram-negative bacteria including Peudomonas aeruginosa. PREPARATION:A compound shown by the formula II (R3 is lower alkyl) or its salt is reacted with a compound shown by the formula III in the presence of an inorganic salt such as sodium iodide, etc. or an organic salt such as sodium p- toluenesulfonate, etc. in the minimum amount of water or water-containing solvent under heating, so that the acyloxyl group at the 3-position of cephem ring of the compound shown by the formula II is converted to a substituted pyridino group.
机译:新材料:由式I表示的化合物(R1为低级烷基; R2为H或低级烷基; Y为5-6元杂环; n为0-2)及其盐。实施例:7β-[2-(2-氨基噻唑-4-基)-2-甲氧基亚氨基乙酰胺基] -3- [4-(咪唑-1-基)吡啶基] -3-头孢-4-羧酸酯。三盐酸盐(syn-异构体)。用途:一种针对革兰氏阳性和革兰氏阴性细菌(包括铜绿假单胞菌)的抗菌剂。制备:在无机盐如碘化钠等或有机盐如对苯二甲酸钠的存在下,使式II所示的化合物(R 3为低级烷基)或其盐与式III所示的化合物反应。 -在加热下以最小量的水或含水溶剂中的甲苯磺酸盐等,使式II所示化合物的头孢烯环的3位的酰氧基转化为取代的吡啶基。

著录项

  • 公开/公告号JPH0244476B2

    专利类型

  • 公开/公告日1990-10-04

    原文格式PDF

  • 申请/专利权人 DAIICHI SEIYAKU CO;

    申请/专利号JP19840077182

  • 发明设计人 EJIMA AKIO;HAYANO TAKESHI;FURUKAWA MINORU;

    申请日1984-04-17

  • 分类号C07D501/46;A61Knull/null;A61K31/545;A61K31/546;A61P31/04;C07Dnull/null;C07D501/00;

  • 国家 JP

  • 入库时间 2022-08-22 06:21:00

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