Affiliation:
1. Département de Chimie, Université Laval
2. Laboratoire de Développement Chimique, Galénique et Pharmacologique des Médicaments LR12ES09, Faculté de Pharmacie, Université de Monastir
Abstract
AbstractA new, simple, and efficient method for the synthesis of 3-aminohydantoins was reported in two steps, starting from the corresponding
l
-amino esters. Commercially available α-amino esters were converted into the corresponding isocyanate derivatives, which were then subjected to the condensation reaction with hydrazine hydrate and arylhydrazines, in the presence of DMAP and DIPEA. This method provides the corresponding 3-aminohydantoins in moderate and good yields under a simple and practical protocol.
Funder
Fonds de recherche du Québec – Nature et technologies
Université Laval
Subject
Organic Chemistry,Materials Science (miscellaneous),Biomaterials,Catalysis