A concise and efficient synthetic approach was developed for the synthesis of functionalized 2,3-disubstituted 1,6-dihydropyrrolo[2,3-g]indazole via a one-pot, three-component reaction promoted by acetic acid in ethanol. The method offers operational simplicity, short reaction time, easy purification, and good to excellent yields.
A concise and efficient synthetic approach was developed for the synthesis of functionalized 2,3-disubstituted 1,6-dihydropyrrolo[2,3-g]indazole via a one-pot, three-component reaction of 1H-indazol-6-amine, arylglyoxal monohydrates, and 4-hydroxy-2H-chromen-2-one or 4-hydroxyquinolin-2(1H)-one promoted by acetic acid in ethanol under reflux conditions. The attractive features of this protocol are operational simplicity, short reaction time, easy purification of products, and good to excellent yields.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据