反应详情

The title compound was prepared using the procedure described in Example 1 using 2-amino-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (0.13 g, 0.44 mmol) and 2-bromo-6-(methylsulfonyl)pyridine (0.10 g, 0.44 mmol) as the starting materials.