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Regioselectivity of the monohalogenation of 4-allyl-3-allylamino-1,2,4-triazole-5-thione

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Chemistry of Heterocyclic Compounds Aims and scope

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.

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Authors and Affiliations

  1. Uzhgorod National University, Uzhgorod, 88000, Ukraine

    S. M. Khripak, M. V. Slivka, R. V. Vilkov, R. N. Usenko & V. G. Lendel

Authors
  1. S. M. Khripak
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  2. M. V. Slivka
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  3. R. V. Vilkov
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  4. R. N. Usenko
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  5. V. G. Lendel
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Correspondence to S. M. Khripak.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 922–926, June, 2007.

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Khripak, S.M., Slivka, M.V., Vilkov, R.V. et al. Regioselectivity of the monohalogenation of 4-allyl-3-allylamino-1,2,4-triazole-5-thione. Chem Heterocycl Compd 43, 781–785 (2007). https://doi.org/10.1007/s10593-007-0126-6

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  • DOI: https://doi.org/10.1007/s10593-007-0126-6

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