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Azaindole derivatives. 61. Electrophilic substitution reactions in 1-benzyl-6-methoxy-7-cyano-5-azaindole and 6-oxo-5-azaindoline

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The electrophilic substitution reactions (nitration, bromination, acylation, and the Mannich and Vilsmeier reactions) of 1-benzyl-6-methoxy-7-cyano-5-azaindole and the nitration and Vilsmeier reaction of 6-hydroxy-5-azaindoline were studied.

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Literature cited

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Authors and Affiliations

  1. S. Ordzhonikidze All-Union Scientific-Research Institute of Pharmaceutical Chemistry, 119021, Moscow

    N. N. Bychikhina, V. A. Azimov & L. N. Yakhontov

Authors
  1. N. N. Bychikhina
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  2. V. A. Azimov
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  3. L. N. Yakhontov
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Additional information

See [1] for Communication 60.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 356–360, March, 1982.

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Bychikhina, N.N., Azimov, V.A. & Yakhontov, L.N. Azaindole derivatives. 61. Electrophilic substitution reactions in 1-benzyl-6-methoxy-7-cyano-5-azaindole and 6-oxo-5-azaindoline. Chem Heterocycl Compd 18, 268–271 (1982). https://doi.org/10.1007/BF00522126

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  • DOI: https://doi.org/10.1007/BF00522126

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