Michael T. Pirnot,Kevin Stone,Timothy J. Wright,David J. Lamberto,Jochen Schoell,Yu‐hong Lam,Kerstin Zawatzky,Xiao Wang,Stephen M. Dalby,Adam J. Fine,Jonathan P. McMullen
The development of a regio- and stereoselective deoxyfluorination process for the manufacture of belzutifan (MK-6482) was challenging because of a combination of particular reaction and engineering sensitivities. These aspects were addressed through a series of mechanistic, range-finding, and mixing studies that enabled a robust process to be established. In particular, mixing studies led to the discovery of a second phase of perfluoro-1-butanesulfonyl fluoride in the reaction at cryogenic temperature, requiring the liquid–liquid dispersion to be controlled sufficiently to minimize the formation of side products. The changes implemented as a result of these investigations culminated in a process executed successfully on the pilot and commercial scales.