NiCl2-catalyzed cascade reaction of isocyanides with functionalized anilines

作者:Wang Gao Nan; Zhu Tong Hao; Wang Shun Yi*; Wei Tian Qi; Ji Shun Jun
来源:Tetrahedron, 2014, 70(43): 8079-8083.
DOI:10.1016/j.tet.2014.08.032

摘要

A NiCl2-catalyzed isocyanide insertion reaction of anilines bearing another nucleophile functional group utilizing TEMPO as oxidant in isopropyl ethanoate (IPA) or THF has been reported. This simple and general method could afford 2-aminobenzimidazole, 2-aminobenzothiazole, 2-aminobenzoxazole, as well as 2-aminobenzo[d][1,3]oxazine in moderate to excellent yields (up to 95% yield).