反应详情

The title compound was prepared in a manner similar to Example 301 using 6-(4-(4-cyano-3-fluoro-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (S)—N,N-dimethylpyrrolidin-3-amine 1H NMR (400 MHz, DMSO-d6) δ ppm 2.09-2.30 (m, 1 H) 2.33 (d, J=2.27 Hz, 4 H) 2.76-2.93 (m, 6 H) 3.52-3.78 (m, 3 H) 3.83-4.00 (m, 2 H) 7.63 (d, J=7.83 Hz, 1 H) 7.74 (t, J=7.58 Hz, 1 H) 8.21 (d, J=7.58 Hz, 3 H) 8.67 (s, 1 H).). ESI-MS m/z [M+H]+ 435.3.