反应详情

The title compound was prepared according to the general procedure in Example 1 using 4-chloro-2-(fluoromethyl)pyrimidine (19.71 mg, 0.13 mmol) and 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (42 mg, 0.13 mmol) as the starting materials.