N-Arylation of azaindoles in LiCl-mediated catalytic CuI reactions

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Abstract

N-Arylation of 5- and 7-azaindoles was achieved in LiCl-mediated catalytic CuI reactions at 120 °C with moderate to high yields. N-Arylation can be performed with various arylhalides, such as phenyl, pyridine, quinoline, thiophen, and thiazole moieties. © 2007.

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Hong, C. S., Seo, J. Y., & Yum, E. K. (2007). N-Arylation of azaindoles in LiCl-mediated catalytic CuI reactions. Tetrahedron Letters, 48(28), 4831–4833. https://doi.org/10.1016/j.tetlet.2007.05.062

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