Facile access to 3,5-disubstituted 1,2,4-thiadiazoles via T3P®-mediated oxidative dimerization of thioamides

Abstract

A series of propyl phosphonic anhydride (T3P®)-mediated oxidative dimerization reactions, of aromatic and aliphatic thioamides, for the efficient synthesis of 3,5-disubstituted 1,2,4-thiadiazoles has been developed. T3P® has been demonstrated to be an efficient, greener, safer and practical reagent for this transformation, affording good yields under mild conditions. Overall, this approach provides an environmentally benign route to 3,5-disubstituted 1,2,4-thiadiazoles.

Graphical abstract: Facile access to 3,5-disubstituted 1,2,4-thiadiazoles via T3P®-mediated oxidative dimerization of thioamides

Supplementary files

Article information

Article type
Paper
Submitted
29 Aug 2025
Accepted
04 Nov 2025
First published
05 Jan 2026

New J. Chem., 2026, Advance Article

Facile access to 3,5-disubstituted 1,2,4-thiadiazoles via T3P®-mediated oxidative dimerization of thioamides

P. Mallesham, Y. SaiKala, M. Ranga, V. Miriyala, P. D. Sanasi, K. S. Ethiraj, S. Yennam and M. Behera, New J. Chem., 2026, Advance Article , DOI: 10.1039/D5NJ03477A

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