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Reaction of aryl-substituted azidopyrimidines with 1,3-dicarbonyl compounds

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Substituted 1-pyrimidyl-4-acyl-1,2,3-triazoles were obtained by the reaction of 2- and 4-azidopyrimidines with aryl substituents with acetyl- or benzoylacetone. An accelerating effect of an o-hydroxyphenylpyrimidine fragment in this reaction, which was explained by the effect of an intramolecular hydrogen bond, was observed.

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Authors and Affiliations

  1. Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, USSR

    V. P. Krivopalov, E. B. Nikolaenkova, V. F. Sedova & V. P. Mamaev

  2. Novosibirsk Branch, All-Union Scientific-Research Institute of Chemical Agents for the Protection of Plants at the Novosibirsk Institute of Organic Chemistry, USSR

    V. P. Krivopalov, E. B. Nikolaenkova, V. F. Sedova & V. P. Mamaev

  3. Siberian Branch, Academy of Sciences of the USSR, 630090, Novosibirsk

    V. P. Krivopalov, E. B. Nikolaenkova, V. F. Sedova & V. P. Mamaev

Authors
  1. V. P. Krivopalov
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  2. E. B. Nikolaenkova
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  3. V. F. Sedova
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  4. V. P. Mamaev
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedininii, No. 10, pp. 1401–1405, October, 1983.

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Krivopalov, V.P., Nikolaenkova, E.B., Sedova, V.F. et al. Reaction of aryl-substituted azidopyrimidines with 1,3-dicarbonyl compounds. Chem Heterocycl Compd 19, 1116–1120 (1983). https://doi.org/10.1007/BF00505770

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  • DOI: https://doi.org/10.1007/BF00505770

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