反应详情

The title compound was prepared according to the general procedure in Example 1 using (4-chloropyrimidin-2-yl)methanol (54.0 mg, 0.37 mmol) and 2-amino-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (100 mg, 0.34 mmol) as the starting materials.