试剂
化学
组合化学
活性成分
硝基苯
立体化学
成分
催化作用
有机化学
药理学
食品科学
医学
作者
Christina G. Connor,Jacob C. DeForest,Phil Dietrich,Nga M.,Kevin M. Doyle,Shane A. Eisenbeis,Elizabeth Greenberg,Sarah H. Griffin,Brian P. Jones,Kris Jones,Michael J. Karmilowicz,Rajesh Kumar,Chad A. Lewis,Emma L. McInturff,J. Christopher McWilliams,R. H. MEHTA,Bao D. Nguyen,Anil M. Rane,Brian Samas,Barbara Sitter,Howard W. Ward,Mark E. Webster
标识
DOI:10.1021/acs.oprd.0c00366
摘要
The development of a commercial route toward the JAK1 inhibitor abrocitinib is described. The application of a late-stage Lossen rearrangement provided the desired cis-diaminocyclobutane, which was subsequently sulfonylated using a novel water-tolerable triazole sulfonylating reagent to provide the active pharmaceutical ingredient.
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