反应详情

The title compound was prepared from butane-1-sulfonic acid ]4-(4-oxo-piperidine-1-yl)-phenyl]-amide (which was obtained in Example 228) and 5-(3-amino-(2S)-2-hydroxy-propoxy)-8-hydroxy-3,4-dihydro-1H-quinolin-2-one (which was obtained in Example 12) according to the procedure of Example 278 as a white solid; 1H NMR (300 MHz, DMSO-d6) δ 0.82 (t, J=7.3 Hz, 3H), 1.20-1.40 (m, 4H), 1.50-1.70 (m, 2H), 1.80-1.95 (m, 2H), 2.39 (t, J=7.3 Hz, 2H), 2.50-2.80 (m, 5H), 2.85 (t, J=7.3 Hz, 2H), 2.85-3.00 (m, 2H), 3.45-3.60 (m, 2H), 3.75-3.85 (m, 3H), 6.44 (d, J=8.7 Hz, 1H), 6.60 (d, J=8.7 Hz, 1H), 6.89 (d, J=9.0 Hz, 2H), 7.04 (d, J=9.0 Hz, 2H), 8.74 (s, 1H); MS (ES) m/z: 546.9 (MH+); HRMS Calcd. for C27H39N4O6S(MH+): 547.2590. Found: 547.2583.