首页> 外国专利> Procedure for the preparation of the acid 7- (4-hydroxy-0 (-N-methylenamino-phenylacetamido) -3- (1,2,3-triazol-5-il-tio-methyl) -3-cefem-4-carboxylic . (Machine-translation by Google Translate, not legally binding)

Procedure for the preparation of the acid 7- (4-hydroxy-0 (-N-methylenamino-phenylacetamido) -3- (1,2,3-triazol-5-il-tio-methyl) -3-cefem-4-carboxylic . (Machine-translation by Google Translate, not legally binding)

机译:制备酸7-(4-羟基-0(-N-亚甲基氨基-苯基乙酰胺基)-3-(1,2,3-三唑-5-il-tio-甲基)-3-cefem-4-的方法羧酸。(由Google翻译进行机器翻译,不具有法律约束力)

摘要

Procedure for the obtaining of acid 7- (4-hydroxy-o (-N-methylenamino-phenylacetamido) -3 (1,2,3-triazol-5-il-tio-methyl) -3-cefem-4-carboxylic, of formula (I), in which r is the group -n = ch, and of its salts with alkaline metals, compounds that have pharmacological applications for the preparation of injectables or syrup, as antibacterials, consists in the reaction of an aqueous dissolution of formula cefatrizine (I), in which r -nh with aqueous formaldehyde, the reaction is carried out at a ph interval comprised between 7.5 and 8 at the ambient temperature. The product obtained is separated and purified by crystallization in isopropanol ice. (Machine-translation by Google Translate, not legally binding)
机译:获得酸7-(4-羟基-o-(-N-亚甲基氨基-苯基乙酰胺基)-3(1,2,3-三唑-5-il-tio-甲基)-3-cefem-4-羧酸的方法,式(I)的化合物,其中r是-n = ch基团,及其与碱金属的盐,具有药理学用途,可用于制备注射剂或糖浆(作为抗菌剂)的化合物,包括式Cefatrizine(I),其中r -nh与甲醛水溶液在室温下以ph值为7.5至8的间隔进行反应。分离得到的产物,并通过在异丙醇冰中结晶进行纯化。由Google翻译,不具有法律约束力)

著录项

  • 公开/公告号ES8300335A1

    专利类型

  • 公开/公告日1982-11-01

    原文格式PDF

  • 申请/专利权人 AUSONIA FARMACEUTICI S.R.L.;

    申请/专利号ES19820508522

  • 发明设计人

    申请日1982-01-05

  • 分类号C07D501/52;A61K31/545;

  • 国家 ES

  • 入库时间 2022-08-22 13:18:47

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