“…Additionally, heteroaryl and polyaryl amines, exemplified by 3-aminopyridine ( 3m ), 5-aminoquinoline ( 3n ), and 1-naphthylamine ( 3o ), were also viable substrates for this protocol, providing the corresponding products in 90, 95, and 92% yields, respectively. Notably, methods for the synthesis of imines through direct methyl activation are rare . In contrast, the features of the protocol, including its metal-free conditions, ease of operation, use of commercially available reagents, and compatibility with a wide range of substituted anilines, highlight its high practicality and generality.…”