Deaminative Chlorination of Aminoheterocycles

23 March 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.


Selective modification of heteroatom-containing aromatic structures is in high demand as it permits rapid evaluation of molecular complexity in advanced intermediates. Inspired by the remarkable selectivity of deaminases in Nature, herein we present a simple methodology that enables the NH2 groups in aminoheterocycles to be conceived as masked modification handles; with the aid of a simple pyrylium reagent and a cheap chloride source, C(sp2)‒NH2 can be converted into C(sp2)‒Cl bonds. The method is characterized by its remarkable substrate scope and wide functional group tolerance, allowing the modification of >20 different classes of heteroaromatic motifs (5- and 6-membered heterocycles), bearing numerous sensitive motifs. The facile conversion of NH2 into Cl in a late-stage fashion enables practitioners to apply Sandmeyer- and Vilsmeier-type transforms without the burden of explosive and unsafe diazonium salts, stoichiometric transition metals, or highly oxidizing and unselective chlorinating agents.


Zincke reaction
deamination reaction
Late-stage functionalizations


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