Synthesis of ([1,2,4]triazolo[4,3-a]pyridin-3-ylmethyl)phosphonates and their benzo derivatives via 5-exo-dig cyclization

A series of novel 3-methylphosphonylated [1,2,4]triazolo[4,3- a ]pyridines was accessed through a 5- exo - dig -type cyclization of chloroethynylphosphonates and commercially available N-unsubstituted 2-hydrazinylpyridines. In addition, 3-methylphosphonylated [1,2,4]triazolo[4,3- a ]quinolines and 1-methylphosphonylated [1,2,4]triazolo[3,4- a ]isoquinolines were synthesized in a similar manner. The presence of a NO 2 group in the starting hydrazinylpyridine induces a Dimroth-type rearrangement leading to 2-methylphosphonylated [1,2,4]triazolo[1,5- a ]pyridines.