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The reaction of N-R-2-cyanothioacetamides with ethyl[(aryl)hydrazono]chloroacetates

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Depending on the nature of the substituents in the starting reagents and the basicity of the medium the cyclization of N-R-2-cyanothioacetamides with ethyl [(aryl)hydrazono]chloroacetates gives 3-aryl-2-cyanomethylidene-5-ethoxycarbonyl-1,3,4-thiadiazoles, 5-arylhydrazono-2-cyanomethylidene-3-phenyl-thiazolidin-4-ones, di[(aryl)hydrazono](ethoxycarbonylmethyl) sulfides, and 5-amino-3-cyano-2-phenyl-amino-4-(N-phenylaminothiocarbonyl)thiophene.

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Authors and Affiliations

  1. Organic Chemistry Institute, Ukraine National Academy of Sciences, Kiev, 02660

    V. N. Britsun, V. N. Bodnar & M. O. Lozinskii

Authors
  1. V. N. Britsun
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  2. V. N. Bodnar
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  3. M. O. Lozinskii
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp 109–114, January, 2007.

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Britsun, V.N., Bodnar, V.N. & Lozinskii, M.O. The reaction of N-R-2-cyanothioacetamides with ethyl[(aryl)hydrazono]chloroacetates. Chem Heterocycl Compd 43, 93–97 (2007). https://doi.org/10.1007/s10593-007-0014-0

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  • DOI: https://doi.org/10.1007/s10593-007-0014-0

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