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An efficient synthesis of 3-triazolyl-2(1H)-quinolones by CuTC-catalyzed azide-alkyne cycloaddition reaction

  • Université Paris-Saclay
  • Laboratoire de Chimie Thérapeutique

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

Abstract

A facile and efficient Cu(I)-catalyzed azide-alkyne cycloaddition reaction for the synthesis of a series of 3-triazolyl-2(1H)-quinolones 3 have been developed using 3-azido-quinolin-2(1H)-one as the coupling partner. The optimized reaction conditions involve the use of eco- friendly ethanol as the solvent in the presence of copper(I) thiophene-2-carboxylate as the catalyst, to afford good to excellent yields of 3-triazolyl-2(1H)-quinolone derivatives of biological interest.

Original languageEnglish
Pages (from-to)155-158
Number of pages4
JournalApplied Organometallic Chemistry
Volume27
Issue number3
DOIs
Publication statusPublished - 1 Mar 2013
Externally publishedYes

Keywords

  • CuTC
  • hsp90 inhibitors
  • quinolin-2(1H)-one
  • triazole

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