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Molecules  2010 

One-Pot Synthesis of 2,3,4-Triarylquinolines via Suzuki-Miyaura Cross-Coupling of 2-Aryl-4-chloro-3-iodoquinolines with Arylboronic Acids

DOI: 10.3390/molecules15107423

Keywords: 2-aryl-4-chloro-3-iodoquinolines, Suzuki-Miyaura cross-coupling, 2,3-diaryl-4-chloroquinolines, 2,3,4-triarylquinolines

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Abstract:

Palladium–catalyzed Suzuki cross-coupling of 2-aryl-4-chloro-3-iodoquinolines with excess arylboronic acids (2.5 equiv.) in the presence of tricyclohexylphosphine afforded the 2,3,4-triarylquinolines in one-pot operation. The incipient 2,3-diaryl-4-chloroquinolines were also prepared and transformed to the primary 4-amino-2,3-diarylquinolines and 2,3-diarylquinolin-4(1H)-ones.

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