Development and Applications of an Amide Linchpin Reagent

Abstract Linchpin reagents are building blocks that can be chemoselectively functionalized to afford products with a common, useful functional group. In this work, we describe the development and validation of the first amide linchpin reagent and demonstrate its use as a doubly electrophilic building block for the synthesis of a variety of amides, including challenging classes. The linchpin reagent was first functionalized via rhodium‐catalyzed electrophilic amination. Selected masked C ‐isocyanate products were then further derivatized with Grignard reagents to produce secondary amides, or tertiary amides if an alkylating agent was added subsequently. The success of this sequence relies on fully controlled reactivity at each electrophilic site, first exploiting the weak N−O bond and then, the ability to form the free isocyanate intermediate in situ. The overall transformation proceeds with high chemoselectivity, demonstrating the ability of this new linchpin reagent to form amides through atypical bond construction. Finally, the potential of this reagent as a more broadly applicable NCO linchpin is demonstrated by the formation of lactams and unsymmetrical ureas.