Réaction #326478

ord-31c600123e1748d0bdce718c87d7acaf

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

Following a procedure analogous to the procedure described in Example 1 using N-{3-[5-(2-chloro-4-pyrimidinyl)-2-(1,1-dimethylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide (110 mg, 0.204 mmol) and [3-(methylthio)propyl]amine (200 mg, 1.90 mmol) the title compound of Step A was obtained (124 mg, 90% yield). MS (ESI): 608.1 [M+H]+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08642759B2uspto-grants-2014_02