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Chemistry of Heterocyclic Compounds

, Volume 26, Issue 5, pp 520–524 | Cite as

Rearrangement of 1-acetylindoxyl oxime to 1-acetyl-2-chloro-3-iminoindoline hydrochloride

  • V. S. Velezheva
  • S. Yu. Ryabova
Article
  • 36 Downloads

Abstract

Rearrangement of 1-acetylindoxyl oxime upon treatment with hydrogen chloride in acetic acid results in the formation of 1-acetyl-2-chloro-3-iminoindoline hydrochloride. Hydrolysis and acylation of the latter have been studied, along with reaction of 1-acetyl-2-chloro-3-(Ω-chloroacetyl)aminoindole with N- and S-nucleophiles.

Keywords

Hydrogen Acetic Chloride Hydrolysis Acetic Acid 
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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Copyright information

© Plenum Publishing Corporation 1990

Authors and Affiliations

  • V. S. Velezheva
    • 1
  • S. Yu. Ryabova
    • 1
  1. 1.S. Ordzhonikidze All-Union Scientific Research Chemical Pharmaceutical InstituteMoscow

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