• Julia I. Nelina-Nemtseva
  • Anna V. Gulevskaya
  • Vitaliy V. Suslonov
  • Alexander D. Misharev

π-Deficient ethynyl hetarenes were used as dipolarophiles in a 1,3-dipolar cycloaddition reaction with azomethine imines (2-arylidene-5-oxopyrazolidin-2-ium-1-ides). Both CuI-catalyzed and catalyst-free thermally induced reactions proceeded with high regioselectivity providing 6-hetaryl-5-aryl-2,3-dihydropyrazolo[1,2-a]pyrazol-1(5H)-ones in moderate to excellent yields. The ethynyl hetarenes (pyridines, pyrazines, quinoxalines, pteridines and pyrimido[4,5-c]pyridazines) with ortho-methyl, ortho-cyano and ortho-alkynyl substituents were applicable to this reaction. 1,3-Dipolar cycloaddition reactions of alkynyl hetarenes with azomethine imines or other 1,3-dipole reagents can be considered as an alternative synthetic approach to heterobiaryls.

Original languageEnglish
Pages (from-to)1101-1109
Number of pages9
JournalTetrahedron
Volume74
Issue number10
DOIs
StatePublished - 8 Mar 2018

    Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

    Research areas

  • 1,3-Dipolar cycloaddition, 6-Hetaryl-5-aryl-2,3-dihydropyrazolo[1,2-a]pyrazol-1(5H)-ones, Azomethine imines, Ethynyl hetarenes, Heterobiaryls

ID: 87282322