Improved Synthesis of 3-(α , α-diphenyl –α- hydroxymethyl)- 4-amino 1,2,4-triazoline-5-thione and Facile Route to 3,6-Disubstituted 1,2,4-triazolo [3,4-b][1,3,4] thiadiazoles(*)

Section: Article
Published
Jun 24, 2025
Pages
11-16

Abstract

The reaction of thiocarbohydrazide (1) with benzilic acid (2) at the melting temperature (160-170 C) allows an improved preparation of 3-(,-diphenyl--hydroxymethyl)-4-amino-1,2,4-triazoline-5-thione (3).
The compound (3) reacts easily with suitable carboxylic acids in presence of phosphorous oxychloride to afford 1,2,4-triazolo [3,4-b] [1,3,4] thiadiazole ring systems (4a-g). The synthesized products were confirmed by physical and spectral methods.

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How to Cite

J. Mohammed, S., سالم, A. Ahmed, B., & بديع. (2025). Improved Synthesis of 3-(α , α-diphenyl –α- hydroxymethyl)- 4-amino 1,2,4-triazoline-5-thione and Facile Route to 3,6-Disubstituted 1,2,4-triazolo [3,4-b][1,3,4] thiadiazoles(*). Rafidain Journal of Science, 20(8), 11–16. https://doi.org/10.33899/rjs.2009.39880