Regioselective hydroamination of unactivated olefins with diazirines as a diversifiable nitrogen source

Qingyu Xing, Preeti P. Chandrachud, Khalilia Tillett and Justin M. Lopchuk ()
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Qingyu Xing: University of South Florida
Preeti P. Chandrachud: H. Lee Moffitt Cancer Center and Research Institute
Khalilia Tillett: University of South Florida
Justin M. Lopchuk: University of South Florida

Nature Communications, 2024, vol. 15, issue 1, 1-10

Abstract: Abstract Nitrogen-containing compounds, such as amines, hydrazines, and heterocycles, play an indispensable role in medicine, agriculture, and materials. Alkylated derivatives of these compounds, especially in sterically congested environments, remain a challenge to prepare. Here we report a versatile method for the regioselective hydroamination of readily available unactivated olefins with diazirines. Over fifty examples are reported, including the protecting group-free amination of fourteen different natural products. A broad functional group tolerance includes alcohols, ketones, aldehydes, and epoxides. The proximate products of these reactions are diaziridines, which, under mild conditions, are converted to primary amines, hydrazines, and heterocycles. Five target- and diversity-oriented syntheses of pharmaceutical compounds are shown, along with the preparation of a bis-15N diazirine validated in the late-stage isotopic labeling of an RNA splicing modulator candidate. In this work, we report using diazirine (1) as an electrophilic nitrogen source in a regioselective hydroamination reaction, and the diversification of the resulting diaziridines.

Date: 2024
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DOI: 10.1038/s41467-024-50254-8

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