Beilstein Journal of Organic Chemistry (Dec 2014)

Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives

  • Fatma Belkessam,
  • Aidene Mohand,
  • Jean-François Soulé,
  • Abdelhamid Elias,
  • Henri Doucet

DOI
https://doi.org/10.3762/bjoc.10.309
Journal volume & issue
Vol. 10, no. 1
pp. 2912 – 2919

Abstract

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Conditions allowing the one pot 2,5-diheteroarylation of 2,5-dibromothiophene derivatives in the presence of palladium catalysts are reported. Using KOAc as the base, DMA as the solvent and only 0.5–2 mol % palladium catalysts, the target 2,5-diheteroarylated thiophenes were obtained in moderate to good yields and with a wide variety of heteroarenes such as thiazoles, thiophenes, furans, pyrroles, pyrazoles or isoxazoles. Moreover, sequential heteroarylation reactions allow the access to 2,5-diheteroarylated thiophenes bearing two different heteroaryl units.

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