反应详情

The title compound was prepared according to the general procedure in Example 1 using 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (1 g, 3.20 mmol) and 4-chloro-2-[2-(trimethylsilyl)ethoxy]pyrimidine (0.739 g, 3.20 mmol) (see J. Het. Chem., 1994, 989-995) as the starting materials.