반응 #326478

ord-31c600123e1748d0bdce718c87d7acaf

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

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]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08642759B2uspto-grants-2014_02