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Azaindole derivatives.

LIV. Synthesis of 2,3-disubstituted 6-azaindoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

1-Hydroxy derivatives of 2,3-disubstituted 6-azaindoles, which were converted to the corresponding 2,3-disubstituted 6-azaindoles, were obtained from the products of condensation of 3-nitro-4-chloropyridine with acetoacetic and benzoylacetic esters and acetylacetone.

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Literature cited

  1. V. A. Azimov, V. G. Granik, R. G. Glushkov, and L. N. Yakhontov, Khim. Geterotsikl. Soedin., No. 3, 355 (1978).

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  2. A. A. Prokopov and L. N. Yakhontov, Khim. Geterotsikl. Soedin., No. 11, 1531 (1977).

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  3. R. T. Coutts and K. W. Hindmarsh, Org. Mass Spectr., 3, 108 (1970).

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Authors and Affiliations

  1. S. Ordzhonikidze All-Union Scientific-Research Pharmaceutical-Chemistry Institute, Moscow

    A. A. Prokopov, L. F. Linberg, T. F. Vlasova, Yu. N. Sheinker & L. N. Yakhontov

Authors
  1. A. A. Prokopov
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  2. L. F. Linberg
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  3. T. F. Vlasova
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  4. Yu. N. Sheinker
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  5. L. N. Yakhontov
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Additional information

See [1] for communication LIII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 492–495, April, 1978.

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Prokopov, A.A., Linberg, L.F., Vlasova, T.F. et al. Azaindole derivatives.. Chem Heterocycl Compd 14, 402–405 (1978). https://doi.org/10.1007/BF00472153

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  • DOI: https://doi.org/10.1007/BF00472153

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