Beilstein Journal of Organic Chemistry (Mar 2018)

High-yielding continuous-flow synthesis of antimalarial drug hydroxychloroquine

  • Eric Yu,
  • Hari P. R. Mangunuru,
  • Nakul S. Telang,
  • Caleb J. Kong,
  • Jenson Verghese,
  • Stanley E. Gilliland III,
  • Saeed Ahmad,
  • Raymond N. Dominey,
  • B. Frank Gupton

DOI
https://doi.org/10.3762/bjoc.14.45
Journal volume & issue
Vol. 14, no. 1
pp. 583 – 592

Abstract

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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.

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