Zhang Min, Liu Hai-Hui, Yao Zhen, Li Rui-Rui, Yang Lei, Liu Xiong-Li, Zhao Jian-Qiang
Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
Innovation Research Center of Chiral Drugs, Institute for Advanced Study, Chengdu University, Chengdu 610106, China.
J Org Chem. 2025 Aug 22;90(33):11802-11810. doi: 10.1021/acs.joc.5c00712. Epub 2025 Aug 12.
A highly enantioselective aza-Friedel-Crafts reaction of benzothiophene-2,3-dione-derived ketimines and indoles catalyzed by BINOL-derived chiral phosphoric acid was developed for the first time. This protocol enabled the synthesis of structurally diverse enantiopure hybrid 3-indolylmethanamine-benzothiophenes featuring a chiral quaternary carbon center adjacent to both N and S atoms, achieving high yields and high to excellent enantioselectivities (up to 99% yield and 99% ee). The reaction exhibits broad substrate scope, high reactivity, simple operation, and mild conditions. Its synthetic utility was demonstrated by scale-up experiments, diverse transformations, and efficient late-stage functionalization of complex bioactive molecules. This work demonstrates an enantioselective aza-Friedel-Crafts alkylation of indoles and ketimines to construct a tetrasubstituted carbon center adjacent to two heteroatoms.
首次开发了由联萘酚衍生的手性磷酸催化的苯并噻吩-2,3-二酮衍生的酮亚胺与吲哚的高度对映选择性氮杂傅克反应。该方法能够合成结构多样的对映体纯的杂化3-吲哚基甲胺-苯并噻吩,其具有与N和S原子相邻的手性季碳中心,实现了高产率和高至优异的对映选择性(高达99%的产率和99%的对映体过量)。该反应具有广泛的底物范围、高反应活性、操作简单和条件温和的特点。通过放大实验、多样的转化以及复杂生物活性分子的高效后期官能团化证明了其合成效用。这项工作展示了吲哚和酮亚胺的对映选择性氮杂傅克烷基化反应,以构建与两个杂原子相邻的四取代碳中心。