反应详情

The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (R)-tetrahydrofuran-3-amine 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.79-1.94 (m, 1 H) 2.03-2.19 (m, 1 H) 2.36 (s, 3 H) 3.56 (dd, J=9.09, 4.04 Hz, 1 H) 3.66 (td, J=8.15, 5.94 Hz, 1 H) 3.75-3.88 (m, 2 H) 4.42 (dtt, J=8.07, 6.29, 6.29, 4.20, 4.20 Hz, 1 H) 7.54-7.63 (m, 1 H) 7.66 (s, 1 H) 7.71 (br. s., 1 H) 8.11 (br. s., 1 H) 8.20-8.62 (m, 2 H) 8.71 (d, J=6.32 Hz, 1 H) 8.80-8.90 (m, 1 H) 13.12 (br. s., 1 H). MS m/z [M+H]+ 390.2