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Chemistry of Heterocyclic Compounds

, Volume 25, Issue 5, pp 528–530 | Cite as

Synthesis and alkylation of 9-ethoxy-1H-pyrrolo[3,2-b]quinoline

  • N. K. Davydova
  • N. P. Solov'eva
  • V. V. Chistyakov
  • N. B. Marchenko
  • R. G. Glushkov
Article
  • 44 Downloads

Abstract

9-Ethoxy-1H-pyrrolo[3,2-b]quinoline has been synthesized by the hydrogenation of 2-[2-(N,N-dimethylamino)vinyl]-3-nitro-4-ethoxyquinoline using Raney nickel. Alkylation using N,N-dimethylchloroethylamine and hydrolysis with HBr gave two isomers whose structures were established using PMR and mass spectrometry.

Keywords

Hydrogenation Nickel Hydrolysis Mass Spectrometry 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

  1. 1.
    R. G. Glushkov, N. K. Davydova, N. P. Solov'eva, and N. B. Marchenko, Khim. Geterotsikl. Soedin., No. 1, 135 (1987).Google Scholar
  2. 2.
    V. V. Takhisov, Practical Mass Spectrometry of Organic Compounds, Leningrad State University, Leningrad (1977).Google Scholar

Copyright information

© Plenum Publishing Corporation 1989

Authors and Affiliations

  • N. K. Davydova
    • 1
  • N. P. Solov'eva
    • 1
  • V. V. Chistyakov
    • 1
  • N. B. Marchenko
    • 1
  • R. G. Glushkov
    • 1
  1. 1.S. Ordzhonikidze All-Union Chemico-pharmaceutical Research InstituteMoscow

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