An Expedient Approach to Pyrazolo[3,4-b ]pyridine-3-carboxamides via Palladium-Catalyzed Aminocarbonylation

Pyrazolo[3,4- b ]pyridine is a privileged scaffold found in many small drug molecules that possess a wide range of pharmacological properties. Efforts to further develop and exploit synthetic methodologies that permit the functionalization of this heterocyclic moiety warrant investigation. To this end, a series of novel 1,3-disubstituted pyrazolo[3,4- b ]pyridine-3-carboxamide derivatives have been prepared by introducing the 3-carboxamide moiety using palladium-catalyzed aminocarbonylation methodology and employing CO gas generated ex situ using a two-chamber reactor (COware (R) ). The functional group tolerance of this optimized aminocarbonylation protocol is highlighted through the synthesis of a range of diversely substituted C-3 carbox-amide pyrazolo[3,4- b ]pyridines in excellent yields of up to 99%.