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[摘要]:A highly practical method for the Synthesis Of fluorinated benzimidazoles was developed by Cul/TMEDA-catalyzed cross-coupling reaction of N-(2-haloaryl)trifluoroacetimidoyl chlorides with primary amines. The present double amination process tolerates the presence of Cl, Br, or I substituent at the 2-position of the phenyl group. |
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