Wang Fang-Jian, Xu Hui, Xin Ming, Zhang Ze
School of Biological and Chemical Engineering, Anhui Polytechnic University, Wuhu, 241000, Anhui, People's Republic of China.
College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, 310014, People's Republic of China.
Mol Divers. 2016 Aug;20(3):659-66. doi: 10.1007/s11030-016-9666-y. Epub 2016 Mar 14.
Under solvent-free high-speed ball milling, an I[Formula: see text]-promoted condensation/cyclization of easily available methyl ketones or 1,3-dicarbonyl compounds with 2-aminopyridines has been developed, which allows the quick assembly of 2,3-substituted imidazo[1,2-a]pyridines (IPs) with broad molecular diversity, including the antiulcer drug zolimidine. The advantages of high yields, good functional group compatibility, short reaction time (within 90 min), free use of heating, solvent and metal, employment of cheap starting materials, and simple work-up procedure make this protocol a very efficient alternative to traditional synthesis of IPs.
在无溶剂高速球磨条件下,已开发出一种碘促进的易得甲基酮或1,3 - 二羰基化合物与2 - 氨基吡啶的缩合/环化反应,该反应能够快速组装具有广泛分子多样性的2,3 - 取代咪唑并[1,2 - a]吡啶(IPs),包括抗溃疡药物佐利米定。该方法具有产率高、官能团兼容性好、反应时间短(90分钟内)、无需加热、无需使用溶剂和金属、起始原料廉价以及后处理步骤简单等优点,使其成为传统IPs合成方法的一种非常有效的替代方法。