Réaction #326512

ord-dbe3407639814189b1b6593b58df261c

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-{5-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-1-methyl-1H-imidazole-4-sulfonamide (75 mg, 0.152 mmol) and [3-(methylthio)propyl]amine (86 mg, 0.817 mmol) the title compound of Step B was obtained as a golden oil (76 mg, 89% yield). MS (ESI): 561.4 [M+H]+.

Source

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