Mechanochemical Ruthenium-Catalyzed Ortho-Alkenylation of N‑Heteroaryl Arenes with Alkynes under Ball-Milling Conditions

The mechanochemical, solvent-free Ru­(II)-catalyzed alkenylation of N-heteroaryl arenes with alkynes has been successfully described. A wide spectrum of arenes bearing N-heteroaryl moieties such as imidazo­[1,2-a]­pyridine, imidazo­[1,2-a]­pyrimidine, benzo­[d]­imidazo­[2,1-b]­thiazole, imidazo­[2,1-b]­thiazole, 2H-indazole, 1H-indazole, 1H-pyrazole, and 1,2,4-oxadiazol-5­(4H)-one as a directing group reacted with various substituted alkynes under ball milling in the presence of [Ru­(p-cymene)­Cl2]2, affording dialkenylated products in moderate to good yields. The reaction of 2,3-dihydro­phthalazine-1,4-dione with 1-phenyl-1-propyne afforded a monoalkenylated product. Similarly, reaction of 2-phenyl­imidazo­[1,2-a]­pyridine with aliphatic terminal alkynes produced a monoalkenylated derivative as the major product along with minor amount of dialkenylated product. The developed method exhibited excellent functional group compatibility, broad substrate scope, shorter reaction times, and no external heating. Moreover, the method can be readily scaled-up as demonstrated by gram-scale synthesis of 2-(2,6-bis­((E)­1-phenyl­prop-1-en-2-yl)­phenyl)­imidazo­[1,2-a]­pyridine.