Journal
ORGANIC PROCESS RESEARCH & DEVELOPMENT
Volume 26, Issue 3, Pages 525-532Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.oprd.1c00232
Keywords
oxidation; through-process; process development; process safety; manufacturing route development; renal cell carcinoma; RCC; hypoxia-inducible factor-2 alpha; HIF-2 alpha
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We developed a modified Kornblum oxidation method mediated by 2-picoline N-oxide to synthesize belzutifan, which addressed the safety and stench issues associated with the original clinical supply route. By using 1,3-dimethoxybenzene and 2,6-lutidine as a robust quench for the crude bromination stream, we enabled a single-solvent through-process that avoided the isolation of a mutagenic intermediate and resulted in a significantly lower process mass intensity. The ketone product was then directly crystallized from the reaction mixture using a ternary-solvent, constant-volume distillation.
We report the development of a modified Kornblum oxidation mediated by 2-picoline N-oxide for the synthesis of belzutifan that circumvented safety and stench problems associated with the original clinical supply route conditions. A robust quench for the crude bromination stream with 1,3-dimethoxybenzene and 2,6-lutidine enabled a single-solvent through-process that avoided the isolation of a mutagenic intermediate and resulted in a significantly lower process mass intensity. A ternary-solvent, constant-volume distillation was then used to crystallize the ketone product directly from the reaction mixture.
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