On triazoles. I. The reaction of N??cyanocarbonimidodithioic acid diesters with hydrazines

J Reiter, T Somorai, G Jerkovich…

Index: Reiter, J.; Somorai, T.; Jerkovich, Gy.; Dvortsak, P. Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 1157 - 1164

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Citation Number: 40

Abstract

Abstract The reaction of N-cyanocarbonimidodithioic acid di (alkyl and aralkyl) esters with different alkyl-, aralkyl-and arylhydrazines to yield 1-substituted-3-R-thio-5-amino-1H-1, 2, 4- triazoles (3) and 2-substituted-3-R-thio-5-amino-2H-1, 2, 4-triazoles (4) was studied. Isolation of the different types of isomeric pairs of 3 and 4 helped to prove the structure of products obtained which made possible correction of some confusion in the literature. The ...

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~83%

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~76%

Triazoles. III. The alkylation of 3??R′??thio??5??amino??1, ...

[Reiter, J.; Somorai, T.; Dvortsak, P.; Bujtas, Gy. Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 385 - 394]