首页> 外国专利> Procedure for the preparation of 6-aminopenicilanico or 7-aminodexacetoxicefalosporanico ácidos derivados. (Machine-translation by Google Translate, not legally binding)

Procedure for the preparation of 6-aminopenicilanico or 7-aminodexacetoxicefalosporanico ácidos derivados. (Machine-translation by Google Translate, not legally binding)

机译:制备6-氨基青霉烯或7-氨基葡糖中毒头孢菌素衍生物的程序。 (通过Google翻译进行机器翻译,没有法律约束力)

摘要

Procedure for the preparation of 6-aminopenicillanic or 7-aminodexacetoxycephalosporanic acids, of the general formula **(See formula)** in which R represents the phenyl group, optionally substituted by a hydroxide group or by 1,4-cyclohexadieniol radical and Y represents the rest of 7-aminodexacetoxycephalosporanic acid characterized by the fact that 6-aminopenicillanic acid or 7-aminodexacetoxicophalosporanic acid reacts in an appropriate solvent with N, N'-bis-trimethylsilylurea at the boiling temperature of the solvent then achieves the reaction of the mixture with the halo-acid salt of the acid halide selected from the group consisting of 2-amino-2-2 (1, 4-cyclohexadienyl) acetic acid, all of them in their D (-) or L (+) forms or a combination of both, and after separating the trimethisilyl group, the desired compound I is obtained. (Machine-translation by Google Translate, not legally binding)
机译:通式为**(参见式)**的6-氨基青松酸或7-氨基右旋乙酰氧基头孢烷酸的制备方法,其中R代表苯基,可选地被羟基或1,4-环己二烯基和Y取代代表7-氨基右旋乙酰氧基头孢菌酸的其余部分,其特征是6-氨基青松酸或7-氨基葡糖毒基邻苯二甲酸在适当的溶剂中与N,N'-双-三甲基甲硅烷基脲在溶剂的沸腾温度下反应,然后实现混合物的反应酰基卤的卤酸盐选自2-氨基-2-2(1,4-环己二烯基)乙酸,全部呈D(-)或L(+)形式,或两者结合,并分离出三甲硅烷基后,得到所需的化合物I。 (通过Google翻译进行机器翻译,没有法律约束力)

著录项

  • 公开/公告号ES448741A1

    专利类型

  • 公开/公告日1977-07-01

    原文格式PDF

  • 申请/专利权人 DOBFAR S. P. A.;

    申请/专利号ES19760448741

  • 发明设计人

    申请日1976-06-10

  • 分类号C07D;

  • 国家 ES

  • 入库时间 2022-08-23 00:28:37

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