Kancharla Papireddy, Dodean Rozalia A, Li Yuexin, Kelly Jane X
Department of Chemistry, Portland State University, Portland, Oregon 97201, United States.
Department of Veterans Affairs Medical Center, Portland, Oregon 97239, United States.
RSC Adv. 2019;9(72):42284-42293. doi: 10.1039/c9ra09478d. Epub 2019 Dec 20.
A microwave-assisted, rapid and efficient method using boron trifluoride etherate (BF.EtO) for the synthesis of acridones, an intramolecular acylation of -phenylanthranilic acid derivatives, has been developed. The reaction proceeds under solvent-free conditions, tolerates a wide range of functional groups, and provides rapid access to a range of acridones in good to excellent yields. Several of the synthesized acridones exhibited potent antimalarial activities against CQ sensitive and multi-drug resistant (MDR) parasites.
已经开发出一种使用三氟化硼乙醚(BF.EtO)的微波辅助、快速且高效的方法来合成吖啶酮,即对苯基邻氨基苯甲酸衍生物进行分子内酰化反应。该反应在无溶剂条件下进行,能耐受多种官能团,并能以良好至优异的产率快速合成一系列吖啶酮。所合成的几种吖啶酮对氯喹敏感和多药耐药(MDR)寄生虫表现出强效抗疟活性。