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A process for the preparation of new antibiotic macrolides

机译:一种新的抗生素大环内酯类药物的制备方法

摘要

Erythromycin antibiotics of the formula: …CHEM… and their pharmaceutically acceptable acid addition salts, wherein R is hydrogen, alkanoyl having two or three carbon atoms and ethyl succinyl: R1 and R2 when considered separately are, respectively, hydroxy and hydrogen; R1 and R2 when considered together are an oxo group; R3 and R4 when considered separately are each hydrogen; and R3 and R4 when considered together are @C = O; processes for their preparation, and pharmaceutical compositions containing them.
机译:下式的红霉素抗生素及其药学上可接受的酸加成盐,其中R为氢,具有两个或三个碳原子的烷酰基和乙基琥珀酰基:当分别考虑时,R1和R2分别为羟基和氢;当一起考虑时,R1和R2是氧代基团;当分开考虑时,R 3和R 4各自为氢;当一起考虑时,R3和R4为@C = O;制备方法以及包含它们的药物组合物。

著录项

  • 公开/公告号ES526323A0

    专利类型

  • 公开/公告日1985-11-16

    原文格式PDF

  • 申请/专利权人 PFIZER INC.;

    申请/专利号ES19830526323

  • 发明设计人

    申请日1983-10-07

  • 分类号C07H17/08;A61K31/70;

  • 国家 ES

  • 入库时间 2022-08-22 07:37:54

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