Pyrrolo-imidazo[1,2-a]pyridine Scaffolds through a Sequential Coupling of N-Tosylhydrazones with Imidazopyridines and Reductive Cadogan Annulation, Synthetic Scope, and Application

A new strategy for the construction of 3-phenyl-1 H -pyrrolo-imidazo[1,2- a ]pyridine backbone is described. The reaction starts from the coupling between N -tosylhydrazones and 2-chloro-3-nitroimidazo[1,2- a ]pyridines leading to the formation of 3-nitro-2-(arylvinyl)imidazo[1,2- a ]pyridine derivatives. Optimization of Cadogan-reductive conditions allowed the conversion of the obtained nitro derivative to a new scaffold of the type 3-aryl-1 H -pyrrolo-imidazo[1,2- a ]pyridine. This method provides rapid access to new libraries in the context of diversity-oriented synthesis, which intends to generate small molecules with a large structure diversity in an efficient manner. Screening of the biological activity of the newly generated compounds leads to the identification of a new promising compound 5cc , which exhibits good antiproliferative activity in the submicromolar range against a human colon cancer cell line.