SALTS OF 2,5-DIMERCAPTO-1,3,4-THIADIAZOLE

Authors

  • З. Куодис Institute of Chemistry, Vilnius
  • А. Рутавичюс Institute of Chemistry, Vilnius
  • С. Валюлене Institute of Chemistry, Vilnius

DOI:

https://doi.org/10.1007/220

Keywords:

monoammonium salt of 2, 5-dimercapto-1, 3, 4-thiadiazole, monopyridinium salt of 2, monohydrazine salt of 2, dihydrazine salt of 2, monoalkylation of salts of 2, 5-di

Abstract

Reaction of 2,5-dimercapto-1,3,4-thiadiazole with ammonia or pyridine gives monoammonium or monopyridinium salts, and the reaction with hydrazine hydrate gives both mono- and dihydrazine salts, which was confirmed by alkylation of the salts obtained. Difference in the chemical shifts of the SCH2R groups was found in the 1H NMR spectra of the mono- and dialkyl-substituted 2,5-dimercapto-1,3,4-thiadiazoles.

Authors: Z. Kuodis, A. Rutavichyus, and S. Valiulene.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (5), pp 598-602

http://link.springer.com/article/10.1007/BF02290852

Published

2013-01-28

Issue

Section

Original Papers