化学
阶段(地层学)
组合化学
药理学
医学
生物
古生物学
作者
Clayton Hardman,Artur K. Mailyan,Guillaume Mata,Joel W. Beatty,Samuel L. Drew,Jeremy Fournier,Jarosław Kalisiak,Brandon R. Rosen,Matthew Epplin,Balint Gal,Kai Yu,Zhang Wang,Karl T. Haelsig,Anh Tran,Manmohan R. Leleti,Jay P. Powers,Kenneth V. Lawson
标识
DOI:10.1021/acs.oprd.4c00497
摘要
Casdatifan (AB521) is a potent and selective inhibitor of HIF-2α, currently under clinical evaluation for the treatment of clear cell renal cell carcinoma (ccRCC). Here, we report the development of a scalable synthesis of casdatifan, which was used to support its preclinical characterization and the initiation of phase 1 clinical studies. A convergent approach to assembling the tetracyclic scaffold and the development of efficient routes to key intermediates enabled the successful delivery of material to meet clinical development timelines. Crucial to the efficiency of the synthesis was the strategic design of synthetic routes that leverage a combination of substrate and catalyst control to set each of the 5 stereocenters found in the molecule with exquisite selectivity.
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