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Environmentally Responsible and Cost-Effective Synthesis of the Antimalarial Drug Pyronaridine.

Joseph R A KincaidRahul D KavtheJuan C CaravezBalaram S TakaleRuchita R ThakoreBruce H Lipshutz
Published in: Organic letters (2022)
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.
Keyphrases
  • ionic liquid
  • systematic review
  • plasmodium falciparum
  • adverse drug
  • genome wide
  • drug induced
  • amino acid
  • emergency department
  • gene expression
  • dna methylation
  • water soluble
  • climate change