Huynh Tien V, Doan Khang V, Luong Ngoc T K, Nguyen Duyen T P, Doan Son H, Nguyen Tung T, Phan Nam T S
Faculty of Chemical Engineering, Ho Chi Minh City University of Technology (HCMUT) 268 Ly Thuong Kiet, District 10 Ho Chi Minh City Vietnam
Vietnam National University Ho Chi Minh City Linh Trung Ward, Thu Duc District Ho Chi Minh City Vietnam.
RSC Adv. 2020 May 14;10(31):18423-18433. doi: 10.1039/d0ra01750g. eCollection 2020 May 10.
A new synthesis of 2-aroylbenzothiazoles iodine-promoted domino transformations of anilines, acetophenones, and elemental sulfur was demonstrated. The highlights of this tandem synthesis are (1) easily available anilines and acetophenones as feedstock; (2) transition metal-free conditions; (3) inexpensive, nontoxic, easy handling, and abundant elemental sulfur as a building block. This synthetic strategy would complement the existing methods in the synthesis of this important heterocyclic scaffold. To our best knowledge, the formation of 2-aroylbenzothiazoles from simple anilines, acetophenones, and elemental sulfur was not previously reported in the literature.
展示了一种2-芳酰基苯并噻唑的新合成方法——碘促进的苯胺、苯乙酮和元素硫的多米诺反应。这种串联合成的亮点包括:(1)以易于获得的苯胺和苯乙酮作为原料;(2)无过渡金属条件;(3)使用廉价、无毒、易于处理且丰富的元素硫作为结构单元。这种合成策略将补充合成这种重要杂环骨架的现有方法。据我们所知,文献中此前未曾报道过由简单的苯胺、苯乙酮和元素硫形成2-芳酰基苯并噻唑的方法。