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Synthesis of 1-arylsulfonyl-4-arylpiperazines with a sterically hindered nitrogen atom

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding piperazines are formed in high yields by alkylation of 1-arenesulfamido-2-arylaminoethanes with dichloroethane in an aqueous alkaline solution of triethylbenzylammonium chloride. Some properties of the synthesized compounds were investigated.

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Literature cited

  1. S. I. Burmistrov and L. G. Romanovskaya, USSR Author's Certificate No. 250133; Byul. Izobr., No. 26, 21 (1969).

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Authors and Affiliations

  1. Dnepropetrovsk Chemical-Engineering Institute, USSR

    S. I. Burmistrov, N. V. Makarevich & L. Ya. Kravchenko

Authors
  1. S. I. Burmistrov
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  2. N. V. Makarevich
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  3. L. Ya. Kravchenko
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 135–137, January, 1976.

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Burmistrov, S.I., Makarevich, N.V. & Kravchenko, L.Y. Synthesis of 1-arylsulfonyl-4-arylpiperazines with a sterically hindered nitrogen atom. Chem Heterocycl Compd 12, 122–125 (1976). https://doi.org/10.1007/BF00473927

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  • DOI: https://doi.org/10.1007/BF00473927

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