Acyl and sulfonyl derivatives of 3, 5-diamino-1-R-1, 2, 4-triazoles

VM Chernyshev, VA Rakitov, VA Taranushich…

Index: Chernyshev; Rakitov; Taranushich; Blinov Chemistry of Heterocyclic Compounds, 2005 , vol. 41, # 9 p. 1139 - 1146

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Citation Number: 11

Abstract

Abstract 3-Acylamino-5-amino-1-R-1, 2, 4-triazoles are formed regioselectively on acylating 3, 5-diamino-1-R-1, 2, 4-triazoles with an equimolar amount of anhydrides, carboxylic acid chlorides, and sulfonyl chlorides. With an excess of anhydride and carboxylic acid chloride 3, 5-diacylamino-1-R-1, 2, 4-triazoles are formed. 3-Acylamino-5-amino-1-R-1, 2, 4-triazoles do not interact with sulfonyl chlorides. The higher reactivity of the 3-amino group towards ...

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