Chemistry of Heterocyclic Compounds

, Volume 7, Issue 6, pp 725–728 | Cite as

α-(3-Indolyl)-β-hydroxyethylamine and its derivatives

  • M. N. Preobrazhenskaya
  • K. G. Zhirnova
  • N. P. Kostyuchenko
  • O. S. Anisimova
  • N. N. Suvorov
Article
  • 19 Downloads

Abstract

The reduction of oximes of 3-hydroxyacetylindole, 3-benzyloxyacetylindole, and 3-ethoxy-acetylindole (mixtures of syn and anti isomers) gave α-(3-indolyl-β-hydroxyethylamine, α-(3-indolyl)-β-benzyloxyethylamine, and α-(3-indolyl)-β-ethoxyethylamine, the structures of which were confirmed by PMR and mass spectrometry.

Keywords

Mass Spectrometry Organic Chemistry Oxime Anti Isomer 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    L. M. Orlova, M. N. Preobrazhenskaya, K. F. Turchin, Z. G. Starostina, and N. N. Suvorov, Zh. Organ. Khim., 5, 738 (1969).Google Scholar
  2. 2.
    M. N. Preobrazhenskaya, L. M. Orlova, Z. G Starostina, S. S. Liberman, G. P. Sukhinina, and N. N. Suvorov, Khim.-Farmats. Zh., No. 10, 5 (1970).Google Scholar
  3. 3.
    M. N. Preobrazhenskaya, L. M. Orlova, S. S Liberman, G. S. Mosina, V. G. Avramenko, N. P. Sorokina, and N. N. Suvorov, Khim.-Farmats. Zh. (1971) (in press).Google Scholar
  4. 4.
    M. N. Preobrazhenskaya, K. B. Kholodkovskaya, and N. N. Suvorov, Khim. Geterotsikl. Soedin., 265 (1965).Google Scholar
  5. 5.
    K. Shaw and A. Millan, J. Org. Chem., 23, 1177 (1958).Google Scholar
  6. 6.
    A. Bothner-By, Advances in Magnetic Resonance, Vol. 1, Academic Press, p. 195.Google Scholar

Copyright information

© Consultants Bureau 1973

Authors and Affiliations

  • M. N. Preobrazhenskaya
    • 1
  • K. G. Zhirnova
    • 1
  • N. P. Kostyuchenko
    • 1
  • O. S. Anisimova
    • 1
  • N. N. Suvorov
    • 1
  1. 1.S. Ordzhonikidze All-Union Scientific-Research Pharmaceutical Chemistry InstituteMoscow

Personalised recommendations