| Literature DB >> 34357668 |
Williams Nicholson1, Fabien Barreteau2, Jamie Leitch3, Riley Payne3, Ian Priestley4, Edouard Godineau2, Claudio Battilocchio2, Duncan L Browne5.
Abstract
The direct mechanochemical amidation of esters - enabled by ball-milling - is herein described. The operationally simple procedure requires inputs of ester, amine, and sub-stoichiometric KOtBu and is applicable to a preparation of a large and diverse library of 78 amide structures with modest to excellent efficiency. Heteroaromatic and heterocyclic components are specifically shown to be amenable to this mechanochemical protocol. This direct synthesis platform has been applied to the synthesis of API's, agrochemicals, and its ability to deliver gram-scale synthesis of active pharmaceuticals and building blocks is demonstrated, all in the absence of a reaction solvent.Entities:
Keywords: Ball milling; amidation; amides; mechanochemistry
Year: 2021 PMID: 34357668 DOI: 10.1002/anie.202106412
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336