Lewis acid mediated, mild C–H aminoalkylation of azoles via three component coupling

Abstract

This manuscript reports the development of a mild, highly functional group tolerant and metal-free C–H aminoalkylation of azoles via a three-component coupling approach. This method enables the C–H functionalization of diverse azole substrates, such as oxazoles, benzoxazoles, thiazoles, benzothiazoles, imidazoles, and benzimidazoles. DFT calculations identify a key deprotonation equilibrium in the mechanism of the reaction. Using DFT as a predictive tool, the C–H aminoalkylation of initially unreactive substrates (imidazoles/benzimidazoles) can be enabled through an in situ protecting/activating group strategy. The DFT-supported mechanistic pathway proposes key interactions between the azole substrate and the Lewis acid/base pair TBSOTf/EtNⁱPr₂ that lead to azole activation by deprotonation, followed by C–C bond formation between a carbene intermediate and an iminium electrophile. Two diverse approaches are demonstrated to explore the amine substrate scope: (i) a DFT-guided predictive analysis of amine components that relates reactivity to distortion of the iminium intermediates in the computed transition state structures; and (ii) a parallel medicinal chemistry workflow enabling synthesis and isolation of several diversified products at the same time. Overall, the presented work enables a metal-free approach to azole C–H functionalization via Lewis acid mediated azole C–H deprotonation, demonstrating the potential of a readily available, Si-based Lewis acid to mediate new C–C bond formations.