反应详情

温度

120 °C

55 mg (0.24 mmol) of 2-chloro-6-(4-fluorophenyl)pyridine-3-carbonitrile, 83 mg (0.28 mmol) of 1-[2-amino-6-(piperidin-3-ylamino)pyridin-3-yl]-2,2,2-trifluoroethanone hydrochloride (Example 13A) and 0.206 ml (1.18 mmol) of N,N-diisopropylethylamine were initially charged in 2 ml of DMSO. The mixture was heated at 120° C. in a microwave for 30 min. The crude product was purified by means of preparative HPLC (method 13). 72 mg (54% of theory) of the product were obtained in solid form.

1. customThe crude product was purified by means of preparative HPLC (method 13)
2. custom72 mg (54% of theory) of the product were obtained in solid form