反应详情

The title compound was prepared analogously to Example 8 by using 2-chloro-8-fluoroquinoline (Combi-blocks) and 2-fluoro-N-methyl-4-(3-(piperidin-4-yl)pyrazin-2-yl)benzamide trihydrochloride (prepared according to Step 2 of Example 1) in Step 3. 1H NMR (400 MHz, chloroFORM-d) δ ppm 1.85 (d, J=11.93 Hz, 2 H) 2.04-2.19 (m, 2 H) 2.91-3.03 (m, 2 H) 3.09 (d, J=4.50 Hz, 3 H) 3.22 (tt, J=11.61, 3.74 Hz, 1 H) 4.72 (d, J=13.50 Hz, 2 H) 6.80 (d, J=7.43 Hz, 1 H) 7.05 (d, J=9.19 Hz, 1 H) 7.08-7.15 (m, 1 H) 7.20-7.25 (m, 1 H) 7.32-7.39 (m, 2 H) 7.44 (dd, J=8.02, 1.37 Hz, 1 H) 7.88 (dd, J=9.19, 1.17 Hz, 1 H) 8.27 (t, J=8.02 Hz, 1 H) 8.50 (d, J=2.35 Hz, 1 H) 8.55 (d, J=2.35 Hz, 1 H). m/z=460 (M+1).