Paladugu Srinu, Mainkar Prathama S, Chandrasekhar Srivari
Department of Organic Synthesis & Process Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India.
Academy of Scientific and Innovative Research (AcSIR), New Delhi 110020, India.
ACS Omega. 2018 Apr 16;3(4):4289-4294. doi: 10.1021/acsomega.8b00476. eCollection 2018 Apr 30.
The FDA-approved drug for the treatment of asthma, zafirlukast, is synthesized engaging multiple catalytic reactions including a new method for the construction of 3-aroylindoles via oxidative cyclization. The highlights include transition-metal and peroxide free C-H bond activation using the stoichiometric amount of sodium persulfate as an oxidizing agent in the construction of 3-aroylindole, avoiding transition metal, with over 28% overall yield. The complete process has a turnaround time of 28 h to get the target molecule starting from substituted aniline, with practically no protecting groups.
美国食品药品监督管理局(FDA)批准的用于治疗哮喘的药物扎鲁司特,是通过多个催化反应合成的,包括一种通过氧化环化构建3-芳酰基吲哚的新方法。其亮点包括在构建3-芳酰基吲哚时,使用化学计量的过硫酸钠作为氧化剂进行无过渡金属和过氧化物的C-H键活化,避免了过渡金属的使用,总产率超过28%。整个过程从取代苯胺开始到得到目标分子的周转时间为28小时,几乎无需保护基团。