Feng Yadong, Li Yudong, Yu Yunliang, Wang Lianhui, Cui Xiuling
Engineering Research Center of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao University Xiamen 361021 P. R. China
RSC Adv. 2018 Feb 23;8(16):8450-8454. doi: 10.1039/c8ra00524a.
Ir-catalysed direct sulfamidation of quinazolinones has been achieved. A series of -diamided quinazolinones were obtained in up to 96% yields. This transformation could proceed smoothly with a low catalyst loading under mild conditions with nitrogen released as the sole byproduct. This approach potentially provides an environmentally benign sulfamidation process for atom/step economic syntheses of useful pharmaceutical molecules or important building blocks.
已实现铱催化的喹唑啉酮直接氨磺酰化反应。一系列二酰胺基喹唑啉酮的产率高达96%。该转化反应在温和条件下以低催化剂用量即可顺利进行,唯一的副产物是释放出的氮气。这种方法有可能为有用药物分子或重要结构单元的原子/步骤经济性合成提供一种环境友好的氨磺酰化过程。