Abstract
Two routes to the antimalarial drug Pyronaridine are described. The first is a linear sequence that includes a two-step, one-pot transformation in an aqueous surfactant medium, leading to an overall yield of 87%. Alternatively, a convergent route utilizes a telescoped three-step sequence involving an initial neat reaction, followed by two steps performed under aqueous micellar catalysis conditions affording Pyronaridine in 95% overall yield. Comparisons to existing literature performed exclusively in organic solvents reveal a 5-fold decrease in environmental impact as measured by E Factors.
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CITATION STYLE
Kincaid, J. R. A., Kavthe, R. D., Caravez, J. C., Takale, B. S., Thakore, R. R., & Lipshutz, B. H. (2022). Environmentally Responsible and Cost-Effective Synthesis of the Antimalarial Drug Pyronaridine. Organic Letters, 24(18), 3342–3346. https://doi.org/10.1021/acs.orglett.2c00944
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