Issue 0, 1967

Transaminations of NN-dimethylformamide azine

Abstract

NN-Dimethylformamide azine, obtained as its hydrochloride by treating hydrazine or NN′-diacylhydrazines with thionyl chloride in dimethylformamide, undergoes transaminations with primary amines, giving 1,2,4-triazoles, and with secondary amines, giving other NN-disubstituted-formamide azines. The initial product of the reaction with aniline is a 1 : 1 adduct.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 1664-1666

Transaminations of NN-dimethylformamide azine

R. K. Bartlett and I. R. Humphrey, J. Chem. Soc. C, 1967, 1664 DOI: 10.1039/J39670001664

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