Pd-Catalyzed highly selective and direct ortho C−H arylation of pyrrolo[2,3-d]pyrimidine derivatives
The first Pd-catalyzed one-pot direct ortho C−H arylation of pyrrolo[2,3-d]pyrimidine derivatives is reported. Many functional groups are well tolerated under this direct C−H arylation condition. This protocol provides a variety of biphenyl-containing pyrrolo[2,3-d]pyrimidines in good to excellent yields, which are potentially of great importance in medicinal chemistry. Diarylation and heteroarylation were both demonstrated to be effective and this methodology was also proved practical by the gram-scale synthesis.