Copper/Bpin-catalyzed C-H difluoroacetylation-cycloamidation of anilines leading to the formation of 3,3-difluoro-2-oxindoles.

An original and efficient synthesis of 3,3-difluoro-2-oxindole derivatives has been developed via copper/Bpin-catalyzed difluoroacetylation of aniline via C-H activation followed by intramolecular amidation. In this method, amino groups in primary, secondary or tertiary anilines act as directing groups, providing ortho-difluoroacetylated products regioselectively. And in the first two cases, further intramolecular amidation affords 3,3-difluoro-2-oxindole derivatives via a one-pot strategy. This method facilitates the synthesis of compound A as a potent and selective EP receptor antagonist in only five steps in 13% yield instead of the previously reported nine steps in overall 4% yield.