Issue 0, 1984

The triethylamine catalyzed reaction of N,N-disubstituted thioamide–bromine adducts with unsubstituted thiobenzamide

Abstract

The reaction of N,N-disubstituted thioamide–bromine adducts with unsubstituted thioamide, followed by treatment with triethylamine, affords novel N′-thiobenzoylamidines along with smaller amounts of secondary products. A mechanism is proposed for the formation of the amidines. The results give an insight into the initial steps of the mechanism by which thioamides are converted into 1,2,4-thiadiazoles.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1984, 897-900

The triethylamine catalyzed reaction of N,N-disubstituted thioamide–bromine adducts with unsubstituted thiobenzamide

A. Corsaro, A. Compagnini, G. Perrini and G. Purrello, J. Chem. Soc., Perkin Trans. 1, 1984, 897 DOI: 10.1039/P19840000897

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