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Synthesis of monosubstituted amides of 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Monosubstituted amides of 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid were obtained when acetoacetic acid anilide and 2-pyridylamide were used in place of acetoacetic ester in the Hantzsch synthesis.

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, Riga

    G. Ya. Dubur, Z. Ya. Ogle & Ya. R. Uldrikis

Authors
  1. G. Ya. Dubur
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  2. Z. Ya. Ogle
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  3. Ya. R. Uldrikis
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1642–1644, December, 1974.

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Dubur, G.Y., Ogle, Z.Y. & Uldrikis, Y.R. Synthesis of monosubstituted amides of 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid. Chem Heterocycl Compd 10, 1443–1445 (1974). https://doi.org/10.1007/BF00474325

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  • DOI: https://doi.org/10.1007/BF00474325

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