Yu Eric, Mangunuru Hari P R, Telang Nakul S, Kong Caleb J, Verghese Jenson, Gilliland Iii Stanley E, Ahmad Saeed, Dominey Raymond N, Gupton B Frank
Department of Chemistry and Department of Chemical and Life Science Engineering, Virginia Commonwealth University, 601 W. Main St., Richmond, VA 23220, USA.
Beilstein J Org Chem. 2018 Mar 8;14:583-592. doi: 10.3762/bjoc.14.45. eCollection 2018.
Numerous synthetic methods for the continuous preparation of fine chemicals and active pharmaceutical ingredients (API's) have been reported in recent years resulting in a dramatic improvement in process efficiencies. Herein we report a highly efficient continuous synthesis of the antimalarial drug hydroxychloroquine (HCQ). Key improvements in the new process include the elimination of protecting groups with an overall yield improvement of 52% over the current commercial process. The continuous process employs a combination of packed bed reactors with continuous stirred tank reactors for the direct conversion of the starting materials to the product. This high-yielding, multigram-scale continuous synthesis provides an opportunity to achieve increase global access to hydroxychloroquine for treatment of malaria.
近年来,已报道了许多用于连续制备精细化学品和活性药物成分(API)的合成方法,从而使工艺效率有了显著提高。在此,我们报告了抗疟药物羟氯喹(HCQ)的高效连续合成方法。新工艺的关键改进包括去除保护基团,与当前商业工艺相比,总产率提高了52%。连续工艺采用填充床反应器和连续搅拌釜式反应器相结合的方式,将起始原料直接转化为产物。这种高产率、多克规模的连续合成方法为增加全球获取羟氯喹以治疗疟疾提供了机会。