A Modular Approach for the Palladium-Catalyzed Synthesis of Bis-heterocyclic Spirocycles

A simple and modular approach toward bis-heterocyclic spirocycles using palladium catalysis is reported. The enclosed methodology leverages a Mizoroki-Heck-type reaction to generate a neopentylpalladium species. This species can undergo intramolecular C-H activation on a wide array of (hetero)aryl C-H bonds, generating a variety of [4.4] and [4.5] bis-heterocyclic spirocycles in up to 95% yield. A diverse range of bis-heterocyclic spirocycles were possible, with 24 examples and 18 different combinations of heterocycles were synthesized. Biologically relevant aza-heterocycles such as purine, pyrazole, (benz)imidazole, (aza)indole, and pyridine were readily incorporated into the spirocyclic core. The reaction was readily scalable to 1 mmol using a lower catalyst loading and number of base equivalents, and the product was purified without the use flash column chromatography.