Visible-Light-Mediated α-Amino Alkylation of Azomethine Imines: An Approach to <i>N</i>-(β-Aminoalkyl)pyrazolidinones

Abstract

Herein, a mild and robust photocatalytic protocol for the combination of amino and pyrazolidinone functionalities through a radical α-amino alkylation of azomethine iminium ions is demonstrated. This method presents a high functional group tolerance providing direct access to a large family of N-(β-aminoalkyl)pyrazolidinones in good to excellent yields, including the late-stage incorporation of the pyrazolidinone moiety to pharmaceutical ingredients. We propose a plausible scenario for the C–C bond-forming step which involves radical addition followed by a spin-center-shift event.

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