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Chemistry of Heterocyclic Compounds

, Volume 13, Issue 4, pp 433–436 | Cite as

Cyclization of N1-aryl-N3-acetyl-p-nitrobenzamidrazones to substituted 1,2,4-triazoles

  • M. O. Lozinskii
  • T. N. Kudrya
  • S. V. Bonadyk
  • P. S. Pel'kis
Article
  • 26 Downloads

Abstract

The reaction of α-acetamido-p-nitroacetophenone with benzenediazonium salts gave N1-aryl-N3-acetyl-p-nitrobenzamidrazones, which are cyclized to 5-methyl-1-aryl-3-(p-nitrobenzoyl)-1,2,4-triazoles. The latter are quaternized at the nitrogen atom in the 4 position.

Keywords

Nitrogen Organic Chemistry Nitrogen Atom Benzenediazonium Benzenediazonium Salt 
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 1977

Authors and Affiliations

  • M. O. Lozinskii
    • 1
  • T. N. Kudrya
    • 1
  • S. V. Bonadyk
    • 1
  • P. S. Pel'kis
    • 1
  1. 1.Institute of Organic ChemistryAcademy of Sciences of the Ukrainian SSRKiev

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