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Synthesis of pyrido [2,3-d]pyrimidines on the basis of 5-formyl-6-aminouracils

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

2,4-Dioxo-1,2,3,4-tetrahydropyrido [2,3-d]pyrimidines, the structures of which were proved by the PMR and the IR spectra, are formed in the condensation of mono- and di-N-alkyl-5-formyl-6-aminouracils with cyanoacetic acid and its esters, acetoacetic ester, and malonic acid dinitrile.

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Authors and Affiliations

  1. Novokuznetsk Scientific-Research Institute of Pharmaceutical Chemistry, 654034, Novokuznetsk

    N. M. Cherdantseva, V. M. Nesterov & T. S. Safonova

Authors
  1. N. M. Cherdantseva
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  2. V. M. Nesterov
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  3. T. S. Safonova
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 834–837, June, 1983.

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Cherdantseva, N.M., Nesterov, V.M. & Safonova, T.S. Synthesis of pyrido [2,3-d]pyrimidines on the basis of 5-formyl-6-aminouracils. Chem Heterocycl Compd 19, 674–677 (1983). https://doi.org/10.1007/BF00523084

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  • DOI: https://doi.org/10.1007/BF00523084

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