Synthesis of [1,2,4]triazolo[4,3-alpha]piperazines via highly reactive chloromethyloxadiazoles

Org Lett. 2005 Mar 17;7(6):1039-42. doi: 10.1021/ol0474406.

Abstract

[reaction: see text] A concise, modular approach for the synthesis of [1,2,4]triazolo[4,3-alpha]piperazines via condensation of highly reactive chloromethyloxadiazoles with ethylenediamines is described. NMR studies of this reaction provide evidence that suggests a novel activation mechanism for electron-deficient chloromethyloxadiazoles.

MeSH terms

  • Catalysis
  • Ethylenediamines / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Oxadiazoles / chemistry*
  • Oxidation-Reduction
  • Piperazines / chemical synthesis*
  • Stereoisomerism
  • Triazoles / chemical synthesis*

Substances

  • Ethylenediamines
  • Oxadiazoles
  • Piperazines
  • Triazoles