首页> 外国专利> METHOD FOR PREPARING THE SUBSTITUTED ISOTHYOL1 UCHEVIN1 The invention relates to the method of obtaining the derivatives of amides, in particular the substituted isothiourea, which has pharmacological activity. The proposed method for producing a substituted isothiourea of the general formula .- ^^ - (^ E,}, t ^ '(^^^^' 'X_LASR ^ where X is hydrogen, lower alkyl, amino or lower alkylthio; b ^ 1; n - 2-5; R— hydrogen, Ci — 4-, alkyl, aryl, or aralkyl; R * is saturated or unsaturated Ci — Cb-alkyl or (CH2) mZ, where m is 1-3; Z is substituted or unsubstituted aryl, hydroxyl, carboxyl, alkyl ^ mino or cyano group; R and R ^ together can form a 5-membered ring; 2A together with the adjacent carbon and nitrogen atoms is an unsaturated 5-6 membered heterocyclic ring, based on the well-known alkylation reaction of group 5 - C = S and consists in the fact that the thiourea of the general formula /? NK. 'South': '™' ^^ Agde A, X, B, n and R have the above meanings, are treated with a compound o

METHOD FOR PREPARING THE SUBSTITUTED ISOTHYOL1 UCHEVIN1 The invention relates to the method of obtaining the derivatives of amides, in particular the substituted isothiourea, which has pharmacological activity. The proposed method for producing a substituted isothiourea of the general formula .- ^^ - (^ E,}, t ^ '(^^^^' 'X_LASR ^ where X is hydrogen, lower alkyl, amino or lower alkylthio; b ^ 1; n - 2-5; R— hydrogen, Ci — 4-, alkyl, aryl, or aralkyl; R * is saturated or unsaturated Ci — Cb-alkyl or (CH2) mZ, where m is 1-3; Z is substituted or unsubstituted aryl, hydroxyl, carboxyl, alkyl ^ mino or cyano group; R and R ^ together can form a 5-membered ring; 2A together with the adjacent carbon and nitrogen atoms is an unsaturated 5-6 membered heterocyclic ring, based on the well-known alkylation reaction of group 5 - C = S and consists in the fact that the thiourea of the general formula /? NK. 'South': '™' ^^ Agde A, X, B, n and R have the above meanings, are treated with a compound o

机译:取代的异硫醇Uchevin1的制备方法本发明涉及获得具有药理活性的酰胺衍生物,特别是取代的异硫脲的方法。提出的制备具有通式.- ^^-(^ E,},t ^'(^^^^'“ X_LASR ^的方法,其中X是氢,低级烷基,氨基或低级烷硫基; b ^ 1; n-2-5; R-氢,C 1-4-,烷基,芳基或芳烷基; R *为饱和或不饱和的C 1 -Cb烷基或(CH2)mZ,其中m为1-3; Z为取代或未取代的芳基,羟基,羧基,烷基^氨基或氰基; R和R ^一起可以形成5元环; 2A与相邻的碳和氮原子一起是不饱和的5-6元杂环,基于5-C = S基团的众所周知的烷基化反应,在于以下事实:通式/?NK的硫脲“ South”:'™'^^ Agde A,X,B,n和R具有以上含义,用复方o

摘要

机译:

著录项

获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号