反应详情

Following the procedure for the preparation of 2-{2-[4-(4-Pyridin-4-yl-2H-pyrazol-3-yl)-phenyl]-ethyl}-quinoline but substituting 2-(2-Chloro-pyridin-4-yl)-1-[4-(quinolin-2-ylmethoxy)-phenyl]-ethanone provided the title compound. 1H NMR (400 MHz, CDCl3) δ 8.23 (m, 2H), 8.08 (d, J=8.7 Hz, 1H), 7.83 (d, J=8.3 Hz, 1H), 7.80 (s, 1H), 7.75 (t, J=7.1 Hz, 1H), 7.67 (d, J=8.3 Hz, 1H), 7.57 (t, J=7.1 Hz, 1H), 7.33 (d, J=9.1 Hz, 2H), 7.05 (m, 4H), 5.40 (s, 2H); MS: (M−H m/z=413.1).