反应详情

The title compound was prepared following the procedure of example two with N5-(2-chloro-pyrimidin-4-yl)-N2-(4-methoxy-benzyl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (82 mg, 0.20 mmol) and 4-(1-Methanesulfonyl-ethyl)-phenylamine (47 mg, 0.20 mmol) as a white solid (49 mg, 40%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.24 (s, 1H), 7.75-7.80 (M, 3H), 7.60 (br s, 1H), 7.34 (d, J=8.7 Hz, 2H), 7.26 (d, J=7.8 Hz, 3H), 7.12 (s, 1H), 6.89 (d, J=8.4 Hz, 3H), 5.66 (d, J=6.0 Hz, 1H), 4.53 (d, J=5.7 Hz, 2H), 4.40 (m, 1H), 3.72 (s, 3H), 3.58 (s, 3H), 3.43 (s, 3H), 2.76 (s, 3H), 1.59 (d, J=7.2 Hz, 3H). MS (ESI) m/z=572 [M+H]+.