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Metal-Free Synthesis of 1,5-Disubstituted 1,2,3-Triazoles.

Andrey BubyrevKsenia MalkovaGrigory KantinDmitry V Dar'inMikhail Yu Krasavin
Published in: The Journal of organic chemistry (2021)
A three-component synthesis of 1,5-disubstituted 1,2,3-triazoles from α-acetyl-α-diazomethane sulfonamides, primary aliphatic amines, and aromatic aldehydes is presented. The 1,2,3-triazoles can be accessed in two alternative variants, depending on the substitutions in the sulfonamide portion of the diazo reagent. In one variant, intermediate 1,2,3-triazoline-4-sulfonamides are isolated chromatographically and then subjected to thermally promoted aromatization with elimination of sulfur(IV) oxide and amine. In the other variant, both chemical transformations take place in a single step conducted at room temperature.
Keyphrases
  • room temperature
  • ionic liquid
  • solid phase extraction
  • copy number
  • mass spectrometry
  • dna methylation
  • genome wide
  • simultaneous determination