Decarboxylative sp3 C–N Coupling via Dual Copper/Photoredox Catalysis

摘要

Over the last three decades, significant progress has been made in the development of methods to construct sp² C–N bonds using palladium, copper, or nickel catalysis^,. However, the incorporation of alkyl substrates to form sp³ C–N bonds remains one of the major challenges in the field of cross-coupling chemistry. Here, we demonstrate that the synergistic combination of copper catalysis and photoredox catalysis can provide a general platform to address this challenge. This cross-coupling system employs naturally abundant alkyl carboxylic acids and commercially available N-nucleophiles as coupling partners, and is applicable to a wide variety of primary, secondary, and tertiary alkyl carboxylic acids (via iodonium activation). At the same time, a vast array of N-nucleophiles, including N-heterocycles, amides, sulfonamides, and anilines, can undergo C–N coupling to provide N-alkyl products in good to excellent efficiency at room temperature and in short order (5 minutes to 1 hour). We have also demonstrated that this C–N coupling protocol can be applied to substrates bearing multiple amines with high regioselectivity, as well as complex drug molecules, enabling the rapid construction of molecular complexity and the late stage functionalization of bioactive pharmaceuticals.