反应详情

The title compound was prepared in a manner similar to Example 213 using 6-(4-bromo-5-methoxy-1H-pyrazol-1-yl)-N-((tetrahydro-2H-pyran-4-yl)methyl)nicotinamide (60.0 mg, 0.152 mmol), (5-fluoro-2-methoxypyridin-4-yl)boronic acid. 1H NMR (400 MHz, DMSO-d6) δ 1.15 (qd, J=12.3, 4.4 Hz, 2 H) 1.55 (d, J=12.9 Hz, 2 H) 1.74 (ddt, J=11.1, 7.4, 3.9, 3.9 Hz, 1 H) 3.13 (t, J=6.3 Hz, 2 H) 3.74-3.82 (m, 5 H) 7.74 (d, J=4.8 Hz, 1 H) 8.03 (d, J=3.0 Hz, 1 H) 8.16 (d, J=2.5 Hz, 1 H 8.30-8.45 (m, 2 H) 8.66 (t, J=5.7 Hz, 1 H) 8.84 (d, J=1.3 Hz, 1 H). MS m/z [M+H]+ 428.5.