Open AccessCatalytic Cyanation of C–N Bonds with CO2/NH3
Author(s) -
Fachao Yan,
JianFei Bai,
Yanan Dong,
Shaoli Liu,
Chen Li,
Chenxia Du,
Yuehui Li
Publication year - 2022
Publication title -
jacs au
Language(s) - English
Resource type - Journals
ISSN - 2691-3704
DOI - 10.1021/jacsau.2c00392
Subject(s) - cyanation , chemistry , regioselectivity , reactivity (psychology) , aryl , catalysis , medicinal chemistry , bond cleavage , yield (engineering) , steric effects , electrophile , organic chemistry , alkyl , combinatorial chemistry , medicine , alternative medicine , materials science , pathology , metallurgy
Cyanation of benzylic C-N bonds is useful in the preparation of important α-aryl nitriles. The first general catalytic cyanation of α-(hetero)aryl amines, analogous to the Sandmeyer reaction of anilines, was developed using reductive cyanation with CO 2 /NH 3 . A broad array of α-aryl nitriles was obtained in high yields and regioselectivity by C-N cleavage of intermediates as ammonium salts. Good tolerance of functional groups such as ethers, CF 3 , F, Cl, esters, indoles, and benzothiophenes was achieved. Using 13 CO 2 , a 13 C-labeled tryptamine homologue (five steps, 31% yield) and Cysmethynil (six steps, 37% yield) were synthesized. Both electronic and steric effects of ligands influence the reactivity of alkyl nickel species with electrophilic silyl isocyanates and thus determine the reactivity and selectivity of the cyanation reaction. This work contributes to the understanding of the controllable activation of CO 2 /NH 3 and provides the promising potential of the amine cyanation reaction in the synthesis of bio-relevant molecules.