反应详情

To a mixture of tert-butyl 4-(((trifluoromethyl)sulfonyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate (I16) (0.504 g, 1.52 mmol), tert-butyl(2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate (I62) (0.496 g, 1.47 mmol), and PdCl2(PPh3)2 (0.055 g, 0.078 mmol) under a N2 atmosphere was added dioxane (15 mL) and the mixture was bubbled with N2 for 5 minutes before addition of 3.0 M aqueous sodium carbonate (1.5 mL, 4.5 mmol). The reaction was heated at reflux for 6 hours then concentrated under reduced pressure. The residue was chromatographed on silica gel (0-25% EtOAc/petroleum benzine 40-60° C.) to give the title compound (I57) (0.409 g, 71%); 1H NMR (400 MHz, CDCl3) δ 7.12 (m, 3H), 6.09 (s, 1H), 4.08 (m, J=2.8 Hz, 2H), 3.63 (dd, J=5.6, 5.6 Hz, 2H), 2.49 (m, 2H), 1.42 (s, 18H).

1. temperatureThe reaction was heated
2. temperatureat reflux for 6 hours
3. concentrationthen concentrated under reduced pressure
4. customThe residue was chromatographed on silica gel (0-25% EtOAc/petroleum benzine 40-60° C.)