Ruthenium-Catalyzed Hydroamination of Unactivated Terminal Alkenes with Stoichiometric Amounts of Alkene and an Ammonia Surrogate by Sequential Oxidation and Reduction

• DOI: 10.1021/jacs.0c11043
• Publication Date: 2020-12-24T16:33:51Z
• Authors: Senjie Ma; Christopher K. Hill; Casey L. Olen; John F. Hartwig
• Keywords: Organic Chemistry; Aminopyridines; Chemical; General Chemistry; Alkenes; 540; 01 natural sciences; Catalysis; Ruthenium; 0104 chemical sciences; Inorganic Chemistry; Engineering; Chemical sciences; Models, Chemical; Models; Coordination Complexes; Chemical Sciences; Oxidation-Reduction; Density Functional Theory; Amination

Hydroamination of alkenes catalyzed by transition-metal complexes is an atom-economical method for the synthesis of amines, but reactions of unactivated alkenes remain inefficient. Additions of N-H bonds to such alkenes catalyzed by iridium, gold, and lanthanide catalysts are known, but they have required a large excess of the alkene. New mechanisms for such processes involving metals rarely used previously for hydroamination could enable these reactions to occur with greater efficiency. We report ruthenium-catalyzed intermolecular hydroaminations of a variety of unactivated terminal alkenes without the need for an excess of alkene and with 2-aminopyridine as an ammonia surrogate to give the Markovnikov addition product. Ruthenium complexes have rarely been used for hydroaminations and have not previously catalyzed such reactions with unactivated alkenes. Identification of the catalyst resting state, kinetic measurements, deuterium labeling studies, and DFT computations were conducted and, together, strongly suggest that this process occurs by a new mechanism for hydroamination occurring by oxidative amination in concert with reduction of the resulting imine.