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A convenient method for the synthesis of substituted 2-alkylthio-3-cyano-4,6-dimethyl-5-phenylcarbamoyl-1,4-dihydropyridines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Substituted 2-alkylthio-3-cyano-4,6-dimethyl-5-phenylcarbamoyl-1,4-dihydropyridines were obtained by successive reaction of acetaldehyde with cyanothioacetamide and acetoacetanilide, α-chloracetamide or phenacyl bromide in the presence of piperidine.

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Authors and Affiliations

  1. Taras Shevchenko Lugansk State Pedagogical University, 348011, Lugansk, Ukraine

    S. G. Krivokolysko & V. D. Dyachenko

  2. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 117913, Moscow, Russia

    V. P. Litvinov

Authors
  1. S. G. Krivokolysko
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  2. V. D. Dyachenko
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  3. V. P. Litvinov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 345–347, March, 2000.

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Krivokolysko, S.G., Dyachenko, V.D. & Litvinov, V.P. A convenient method for the synthesis of substituted 2-alkylthio-3-cyano-4,6-dimethyl-5-phenylcarbamoyl-1,4-dihydropyridines. Chem Heterocycl Compd 36, 284–286 (2000). https://doi.org/10.1007/BF02256865

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  • DOI: https://doi.org/10.1007/BF02256865

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