作者
Liang Zhang,Daniel J. Griffin,Matthew G. Beaver,Laura E. Blue,Christopher J. Borths,Derek B. Brown,Seb Caille,Ying Chen,Alan H. Cherney,Brian M. Cochran,John Colyer,Michael T. Corbett,Tiffany L. Correll,Richard Crockett,Xi‐Jie Dai,Peter K. Dornan,Robert Farrell,Simon J. Hedley,Hsiao‐Wu Hsieh,Liang Huang,Seth Huggins,Min Liu,Michael A. Lovette,Kyle W. Quasdorf,William Powazinik,Jonathan Reifman,Jo Anna Robinson,Rahul P. Sangodkar,Sonika Sharma,Srividya Sharvan Kumar,Austin G. Smith,Gabrielle St‐Pierre,Jason S. Tedrow,Oliver R. Thiel,Jonathan V. Truong,Shawn D. Walker,Carolyn S. Wei,Ashraf Wilsily,Yong Xie,Ning Yang,Andrew T. Parsons
摘要
A commercial process to manufacture sotorasib (AMG 510), a first-in-class KRASG12C inhibitor, is described. Development efforts focused on rendering a fit-for-purpose early-phase route into a viable long-term commercial process through the reduction of side reactions to improve yield and product quality, as well as reducing cycle times of crystallization processes by improving particle properties and filtration times. These improvements were key to ensuring clinical supply and commercial launch. The final route consists of five synthetic operations from starting material M-1, including a telescoped two-step sequence, and a final form-setting crystallization.