反应详情

The title compound was prepared in a manner similar to Example 112 using 6-(5-hydroxy-4-(2-methoxypyridin-4-yl)-1H-pyrazol-1-yl)nicotinic acid and 4-methoxybutan-2-amine 1H NMR (400 MHz, methanol-d4) δ ppm 1.28 (d, J=6.32 Hz, 3 H) 1.86 (dd, J=6.95, 5.43 Hz, 2 H) 3.33 (s, 3 H) 3.44-3.57 (m, 2 H) 4.18 (s, 3 H) 4.22-4.34 (m, 1 H) 7.77 (d, J=5.31 Hz, 1 H) 7.86 (s, 1 H) 8.04 (d, J=6.57 Hz, 1 H) 8.44 (br. s., 3 H) 8.68-9.15 (m, 1 H). MS m/z [M+H]+ 398.2.