反应详情

Following general procedure F, {6-bromo-4-[3-(2-(pyrrolidin-1-yl)ethyl)phenylamino]quinolin-3-yl}ethanone (53 mg, 0.120 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (52 mg, 0.180 mmol) to afford the desired product (31 mg, 50%) as a yellow solid: 1H NMR (300 MHz, CD3OD+TFA-d) δ 9.31 (s, 1H), 8.21 (dd; J=8.8, 2.0 Hz, 1H), 8.00 (d, J=8.8 Hz, 1H), 7.73 (s, 1H), 7.69-7.58 (m, 2H), 7.53 (s, 1H), 7.44-7.38 (m, 1H), 7.10 (s, 2H), 3.72-3.63 (m, 2H), 3.46-3.39 (m, 2H), 3.25-3.14 (m, 2H), 3.14-3.04 (m, 2H), 2.82 (s, 3H), 2.19-2.08 (m, 2H), 2.08-1.97 (m, 2H); ESI MS m/z 520[C29H27Cl2N3O2+H]+; HPLC 97.5% (AUC), tR=10.62 min.