Design and Synthesis of N1,N5-bis[4-(5-Alkyl-1,2,4-oxadiazol-3-yl)phenyl]glutaramides as Potential Antifungal Prodrugs
作者:Nageswara Kode、Jean Vanden Eynde、Annie Mayence、Guangdi Wang、Tien Huang
DOI:10.3390/molecules180911250
日期:——
A facile three step synthesis of a group of N1,N5-bis[4-(5-alkyl-1,2,4-oxadiazol-3-yl)phenyl]glutaramides, N1,N5-bis[4-(1,2,4-oxadiazol-3-yl)phenyl]glutaramide and N1,N5-bis[4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]glutaramide is described. These products are designed to function as masked bis-amidine prodrugs of a promising N1,N5-bis[4-(N'-(carbamimidoyl)phenyl]glutaramide antifungal lead.
本文介绍了一种简便的三步合成N1,N5-双[4-(5-烷基-1,2,4-恶二唑-3-基)苯基]戊二酰胺、N1,N5-双[4-(1,2,4-恶二唑-3-基)苯基]戊二酰胺及N1,N5-双[4-(5-氧代-4,5-二氢-1,2,4-恶二唑-3-基)苯基]戊二酰胺的方法。这些产物旨在作为有前景的N1,N5-双[4-(N'-(氨基甲亚胺酸基)苯基]戊二酰胺抗真菌先导化合物的隐蔽双胍前药。