首页> 外国专利> PROCEDURE FOR FRAMSTAELLNING AV 1,2,3-THIADIAZOLE-5-YLKARBAMIDER

PROCEDURE FOR FRAMSTAELLNING AV 1,2,3-THIADIAZOLE-5-YLKARBAMIDER

机译:1,2,3-噻二唑-5-基氨基甲酸酯的制备方法

摘要

1,2,3-Thiadiazol-5-yl ureas of the formula:- IMAGE wherein R1 represents hydrogen or alkyl optionally interrupted by one or more oxygen and/or sulphur atoms, and R2 represents alkyl optionally interrupted by one or more oxygen and/or sulphur atoms, or a cycloalkyl radical optionally substituted by one or more alkyl radicals, an aromatic hydrocarbon radical optionally substituted by one or more substituents selected from alkyl, halogen, alkylthio, alkoxy, trifluoromethyl and nitro, or an optionally substituted N-containing heterocyclic radical or NR1R2 represents morpholino, piperidino or pyrrolidino, are prepared by reacting a compounds:- IMAGE with amines (R1-NH-R2) in inert organic solvents. Preferably the compound II is formed in the reaction mixture. The process of the invention makes it possible to prepare the ureas in a safe and technically simple manner in virtually quantitative yields and good purity. Previously the preparations required the use of 5-amino-1,2,3- thiadiazole which is not easily obtained and is not completely harmless.
机译:式:-的1,2,3-噻二唑-5-基脲,其中R1代表氢或任选被一个或多个氧和/或硫原子间断的烷基,R2代表任选被一个或多个氧间断的烷基和/或硫原子,或任选被一个或多个烷基取代的环烷基,任选被一个或多个选自烷基,卤素,烷硫基,烷氧基,三氟甲基和硝基的取代基取代的芳族烃基,或任选取代的N-含有杂环基或NR1R2的化合物表示吗啉代,哌啶子基或吡咯烷基,是通过使化合物:与胺(R1-NH-R2)在惰性有机溶剂中反应制备的。优选在反应混合物中形成化合物II。本发明的方法使得可以以安全和技术上简单的方式以实际上定量的产率和良好的纯度制备脲。以前,这些制剂需要使用5-氨基-1,2,3-噻二唑,这种化合物不易获得,而且也不是完全无害的。

著录项

  • 公开/公告号FI792770A

    专利类型

  • 公开/公告日1980-03-23

    原文格式PDF

  • 申请/专利权人 SCHERING AG;

    申请/专利号FI19790002770

  • 发明设计人 KRUEGER HANS-RUDOLF;

    申请日1979-09-06

  • 分类号C07D;

  • 国家 FI

  • 入库时间 2022-08-22 18:33:09

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