A series of heterobiaryl amides was designed and synthesized as novel mGluR5 antagonists. The synthesis using palladium catalyzed Suzuki–Miyaura cross-coupling reactions provided an array of compounds with a range of in vitro activities. In particular, compound 9e, 4 (3, 5-difluorophenyl)-N-(6-methylpyridin-1-yl) picolinamide, exhibited nanomolar affinity at the mGluR5 and will serve as a template for future drug design.