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Chemistry of Heterocyclic Compounds

, Volume 14, Issue 3, pp 289–293 | Cite as

Azaindole derivatives

LIII. New method for the synthesis of 6-chloro-5-azaindoline
  • V. A. Azimov
  • V. G. Granik
  • R. G. Glushkov
  • L. N. Yakhontov
Article

Abstract

1-Benzyl-6-hydroxy-7-cyano-5-azaindoline, which was converted to 6-chloro-5-azaindoline through 6-hydroxy-5-azaindoline, was synthesized from O-methylbutyrolactim through 1-benzyl-2-pyrrolidone, 1-benzyl-2-cyano (carbamoylmethylene)-pyrrolidine, and the product of its condensation with dimethylformamide diethylacetal.

Keywords

Organic Chemistry Dimethylformamide Pyrrolidine Diethylacetal Azaindole 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature cited

  1. 1.
    A. A. Prokopov and L. N. Yakhontov, Khim. Geterotsikl. Soedin., No. 11, 1531 (1977).Google Scholar
  2. 2.
    V. G. Granik, N. B. Marchenko, T. F. Vlasova, and R. G. Glushkov, Khim. Geterotsikl. Soedin., No. 11, 1509 (1976).Google Scholar
  3. 3.
    L. N. Yakhontov and E. I. Lapan, Khim. Geterotsikl. Soedin., No. 1, 27 (1970).Google Scholar

Copyright information

© Plenum Publishing Corporation 1978

Authors and Affiliations

  • V. A. Azimov
    • 1
  • V. G. Granik
    • 1
  • R. G. Glushkov
    • 1
  • L. N. Yakhontov
    • 1
  1. 1.S. Ordzhonikidze All-Union Scientific-Research Pharmaceutical-Chemistry InstituteMoscow

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