6-Halo-2-pyridone as an efficient organocatalyst for ester aminolysis. Issue 40 (14th July 2021)

• Record Type: Journal Article
• Authors: Yamada, Takeshi; Watanabe, Yusuke; Okamoto, Sentaro
• Is Part Of: RSC advances. Volume 11:Issue 40(2021)
• Page Start: 24588
• Page End: 24593
• Publication Date: 2021-07-14
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra04651a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : 6-Halo-2-pyridones effectively catalyse ester aminolysis as bifunctional catalysts. This reaction did not require any special conditions and was operationally convenient. Abstract : It was found that 6-halo-2-pyridones catalysed ester aminolysis in which not only reactive aryl esters but also relatively less reactive methyl and benzyl esters could be used as a substrate. The reaction could be performed without strictly dry and anaerobic conditions and the 6-chloro-2-pyridone catalyst could be recovered quantitatively after reaction. The method could be applied to dipeptide synthesis from methyl or benzyl esters of amino acids, where a high enantiomeric purity of the products was maintained. The mechanism involving dual activation of ester and amine substrates through hydrogen bonding between catalyst and substrates is proposed where 6-halo-2-pyridones act as a bifunctional Brønsted acid/base catalyst.