反应详情

The title compound, as a TFA salt, was prepared in a manner similar to Example 74 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (1-methylpyrrolidin-3-yl)methanamine 1H NMR (400 MHz, DMSO-d6) δ ppm 1.61-1.97 (m, 1H) 1.98-2.29 (m, 1 H) 2.40-2.47 (m, 3 H) 2.54-2.65 (m, 1 H) 2.73-2.91 (m, 4 H) 2.97-3.25 (m, 1 H) 3.40 (dt, J=18.51, 6.28 Hz, 2 H) 3.50-3.78 (m, 2 H) 7.67 (d, J=7.33 Hz, 1 H) 7.70-7.89 (m, 2 H) 8.12-8.32 (m, 1 H) 8.33-8.74 (m, 2 H) 8.77-8.98 (m, 2 H) 9.66-9.94 (m, 1 H) 12.62-13.68 (m, 1 H). MS m/z [M+H]+ 417.2.