Development of a Scalable Synthesis for the Potent Kinase Inhibitor BMS-986236; 1‑(5-(4-(3-Hydroxy-3-methylbutyl)‑1H‑1,2,3-triazol-1-yl)-4-(isopropylamino)pyridin-2-yl)‑1H‑pyrazolo[3,4‑b]pyridine-5-carbonitrile
A scalable route to 1-(5-(4-(3-hydroxy-3-methylbutyl)-1H-1,2,3-triazol-1-yl)-4-(isopropylamino)pyridin-2-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile (1, BMS-986236) was developed by incorporating an alternate azide intermediate following safety-driven processes. The newly developed process invo...
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Veröffentlicht in: | Organic process research & development 2019-05, Vol.23 (5), p.912-918 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A scalable route to 1-(5-(4-(3-hydroxy-3-methylbutyl)-1H-1,2,3-triazol-1-yl)-4-(isopropylamino)pyridin-2-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile (1, BMS-986236) was developed by incorporating an alternate azide intermediate following safety-driven processes. The newly developed process involved mitigating safety hazards and eliminating the column chromatography purification. The issue of trace metal contamination in the final API observed in the first-generation synthesis has been overcome. |
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ISSN: | 1083-6160 1520-586X |
DOI: | 10.1021/acs.oprd.9b00023 |