Beilstein Journal of Organic Chemistry (Dec 2011)

Efficient synthesis of 1,3-diaryl-4-halo-1H-pyrazoles from 3-arylsydnones and 2-aryl-1,1-dihalo-1-alkenes

  • Yiwen Yang,
  • Chunxiang Kuang,
  • Hui Jin,
  • Qing Yang,
  • Zhongkui Zhang

DOI
https://doi.org/10.3762/bjoc.7.195
Journal volume & issue
Vol. 7, no. 1
pp. 1656 – 1662

Abstract

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An efficient synthesis of 1,3-diaryl-4-halo-1H-pyrazoles was achieved. The synthesis involves the [3 + 2] dipolar cycloaddition of 3-arylsydnones and 2-aryl-1,1-dihalo-1-alkenes. The process proceeds smoothly in moderate to excellent yields. 1,3-Diaryl-4-halo-1H-pyrazoles are found to be important intermediates that can easily be converted into 1,2,5-triaryl-substituted pyrazoles via Pd-catalyzed C–H bond activation.

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