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Chemistry of Heterocyclic Compounds

, Volume 15, Issue 1, pp 76–78 | Cite as

Azaindole derivatives

56. Synthesis of 4-bromo-6-azaindole
  • A. A. Prokopov
  • L. N. Yakhontov
Article

Abstract

3-Bromo-5-nitro-4-(β-dimethylaminovinyl) pyridine, the reduction of which with iron filings in acetic acid led to 4-bromo-6-azaindole, was obtained from 3-bromo-4-chloro-5-nitropyridine via (3-bromo-5-nitro-4-pyridyl)malonic ester and 3-bromo-5-nitro-4-methylpyridine.

Keywords

Iron Acetic Ester Acetic Acid Organic Chemistry 
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

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    A. A. Prokopov and L. N. Yakhontov, Khim. Geterotsikl. Soedin., No. 4, 496 (1978).Google Scholar
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    A. A. Prokopov, L. F. Linberg, T. F. Vlasova, Yu. N. Sheinker, and L. N. Yakhontov, Khim. Geterotsikl. Soedin., No. 4, 492 (1978).Google Scholar
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    E. Koenigs and A. Fulde, Ber., 60, 2106 (1927).Google Scholar
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Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • A. A. Prokopov
    • 1
  • L. N. Yakhontov
    • 1
  1. 1.S. Ordzhonikidze All-Union Scientific-Research Pharmaceutical-Chemistry InstituteMoscow

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