Ludwig-Maximilians-Universität München, Department Chemie, Butenandtstrasse 5-13, Haus F, 81377, München, Germany.
Angew Chem Int Ed Engl. 2018 Jan 22;57(4):1108-1111. doi: 10.1002/anie.201710931. Epub 2017 Dec 28.
Aryl- and heteroarylzinc pivalates can be aminated with O-benzoylhydroxylamines at 25 °C within 2-4 h in the presence of 2.5-5.0 % CoCl ⋅2 LiCl to furnish the corresponding tertiary arylated or heteroarylated amines in good yields. This electrophilic amination also provides access to diarylamines and aryl(heteroaryl)amines. A new tuberculosis drug candidate (Q203) was prepared in six steps and 56 % overall yield by using this cobalt-catalyzed amination as the key step.
芳基和杂芳基锌特戊酸酯在 25°C 下,在 2.5-5.0%CoCl ⋅2LiCl 的存在下,可以与邻苯甲酰基羟胺反应,在 2-4 小时内反应得到相应的叔芳基或杂芳基胺,产率良好。这种亲电胺化反应也可以得到二芳基胺和芳基(杂芳基)胺。使用这种钴催化的胺化反应作为关键步骤,通过六步反应以 56%的总收率制备了一种新的结核病候选药物(Q203)。