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IMPROVMENTS IN OR RELATING TO PENICILLINS

机译:青霉素类或与青霉素类有关的改进

摘要

alpha -Aminoacylpenicillin antibiotics such as ampicillin and amoxycillin may be prepared in particularly simple manner by a process which comprises preparing a solution of 6-aminopenicillanic acid (6-APA) in a water-immiscible organic solvent by treating 6-APA with an excess of a strong tertiary amine base in the presence of said solvent; neutralising the residual strong tertiary amine base in said solution; reacting the neutralised solution with a solution in a water-immiscible organic solvent of an acylating agent which is a mixed anhydride of a lower alkoxyformic acid and an N-protected derivative of an alpha -aminoacid wherein the N-protecting group is acid-labile, to yield a solution of an N-protected alpha -aminoacylpenicillin derivative; contacting the resulting solution with water and a strong acid to cleave the acid-labile N-protecting group; and isolating the thus-obtained alpha -aminoacylpenicillin from the resulting water-containing system. The use of water-immiscible solvents in the process obviates the need for a solvent evaporation stage during isolation of the alpha -aminoacylpenicillin product and thus renders the process of particular advantage in plant-scale operations.
机译:可以通过以下方法以特别简单的方式制备α-氨基氨苄青霉素抗生素,例如氨苄西林和阿莫西林,该方法包括通过用过量的6-APA处理6-APA来制备与水不混溶的有机溶剂中的6-氨基青霉酸(6-APA)溶液。在所述溶剂存在下的强叔胺碱;中和所述溶液中残余的强叔胺碱;使中和后的溶液与酰化剂在水不混溶的有机溶剂中的溶液反应,该酰化剂是低级烷氧基甲酸的酸酐和α-氨基酸的N-保护的衍生物的混合酸酐,其中N-保护基对酸不稳定,得到N-保护的α-氨基酰基青霉素衍生物的溶液;使所得溶液与水和强酸接触以裂解酸不稳定的N-保护基;从所得的含水系统中分离出由此获得的α-氨基酰基肾上腺素。在该方法中使用与水不混溶的溶剂避免了在分离α-氨基酰基青霉素产物期间进行溶剂蒸发步骤的需要,因此使该方法在工厂规模的操作中具有特别的优势。

著录项

  • 公开/公告号IE41292B1

    专利类型

  • 公开/公告日1979-12-05

    原文格式PDF

  • 申请/专利权人 GLAXO LABORATORIES LTD;

    申请/专利号IE19750001034

  • 发明设计人

    申请日1975-05-08

  • 分类号C07D499/68;

  • 国家 IE

  • 入库时间 2022-08-22 18:32:08

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