REGIOSELECTIVITY OF THE MONOHALOGENATION OF 4-ALLYL-3-ALLYLAMINO-1,2,4-TRIAZOLE-5-THIONE

Authors

  • С. М. Хрипак Uzhgorod National University, Uzhgorod 88000
  • М. В. Сливка Uzhgorod National University, Uzhgorod 88000
  • Р. В. Вилков Uzhgorod National University, Uzhgorod 88000
  • Р. H. Усенко Uzhgorod National University, Uzhgorod 88000
  • В. Г. Лендел Uzhgorod National University, Uzhgorod 88000

DOI:

https://doi.org/10.1007/7507

Keywords:

4-allyl-3-allylamino-1, 2, 4-triazole-5-thione, halogen, [1, 3]thiazolo[2, 3-c][1, 4]triazole, regioselectivity

Abstract

The monohalogenation of 4-allyl-3-allylamino-1,2,4-triazole-5-thione has been studied.  It  was established that the action of bromine and iodine on 4-allyl-3-allylamino-1,2,4-triazole-5-thione at low temperatures leads to selective closure of a thiazoline ring.

How to Cite
Khripak, S. M.; Slivka, M. V.; Vilkov, R. V.; Usenko, R. N.; Lendel, V. G.  Chem. Heterocycl. Compd. 2007, 43, 781. [Khim. Geterotsikl. Soedin. 2007, 922.]

For this article in the English edition see DOI 10.1007/s10593-007-0126-6


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Published

2023-03-03

Issue

No. 6 (2007)

Section

Original Papers