4.4 Article

An efficient access to 2,3-diarylimidazo[1,2-a]pyridines via imidazo[1,2-a]pyridin-2-yl triflate through a Suzuki cross-coupling reaction-direct arylation sequence

Journal

TETRAHEDRON LETTERS
Volume 53, Issue 3, Pages 297-300

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2011.11.015

Keywords

Imidazo[1,2-a]pyridines; Suzuki-Miyaura reaction; Direct arylation; 2,3-Diarylimidazo[1,2-]pyridines; Triflate

Funding

  1. Region des Pays de la Loire

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An efficient method to prepare 2,3-diarylimidazo[1,2-alpha]pyridines is described. The procedure involves a Suzuki cross-coupling reaction followed by a direct arylation at position 3. Imidazo[1,2-alpha]pyridin-2-yl triflate was identified as a suitable coupling partner, permitting access to a variety of highly functionalized 2,3-diarylimidazo[1,2-alpha]pyridines. (C) 2011 Elsevier Ltd. All rights reserved.

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