作者
Xiaobin Liang,Xiaorong Zhou,Yian Luo,An Su,Hanqi Zhou,Jianli Chen,Fengfan Liu,Weike Su
摘要
Tivozanib and cabozantinib are important oral tyrosine kinase inhibitors for the clinical treatment of advanced renal cell carcinoma. In this study, 4-chloro-6,7-dimethoxyquinoline, a common intermediate for two drug syntheses, was designed to be prepared from readily available 1,2-dimethoxybenzene through a sequence of Friedel–Crafts acylation, nitration, hydrogenation, and chlorination. Furthermore, the fully continuous-flow technology was applied to optimize the process and reduce safety risks, achieving the four-step “end-to-end” reaction by concatenating the synthesis, quenching, and phase-separation steps. In the nitration step, the byproduct of 3,4-dimethoxynitrobenzene could isolate by recrystallization. A kinetic model for the nitration reaction was established, indicating that >99% conversion could be achieved at 30 °C with a residence time of 6 min. In the chlorination step, triphosgene (BTC) was used in place of conventional chlorinating reagents (POCl 3, (COCl) 2 ), enabling one-step synthesis of 4-chloro-6,7-dimethoxyquinoline in 73% isolated yield with 99% HPLC purity. Compared with the batch process, the fully continuous-flow synthesis of 4-chloro-6,7-dimethoxyquinoline shortened the total reaction time from 480 to 70 min, increased the overall yield from 46.6% to 53.7%, and reduced PMI by 26%.