3-甲氧基丁-1-胺

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 3-methoxybutan-1-amine 1H NMR (400 MHz, DMSO-d6) δ ppm 1.05 (d, J=6.32 Hz, 3 H) 1.52-1.70 (m, 2 H) 3.17 (s, 3 H) 3.26-3.36 (m, 3 H) 7.72 (d, J=8.59 Hz, 2 H) 8.07 (d, J=6.57 Hz, 2 H) 8.27-8.50 (m, 2H) 8.61 (t, J=5.43 Hz, 2 H) 8.76-8.96 (m, 1 H) 13.46 (br. s., 1 H). MS m/z [M+H]+ 392.1.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 3-methoxybutan-1-amine 1H NMR (400 MHz, DMSO-d6) δ ppm 1.05 (d, J=6.32 Hz, 3 H) 1.52-1.70 (m, 2 H) 3.17 (s, 3 H) 3.26-3.36 (m, 3 H) 7.72 (d, J=8.59 Hz, 2 H) 8.07 (d, J=6.57 Hz, 2 H) 8.27-8.50 (m, 2H) 8.61 (t, J=5.43 Hz, 2 H) 8.76-8.96 (m, 1 H) 13.46 (br. s., 1 H). MS m/z [M+H]+ 392.1.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 3-methoxybutan-1-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.05 (d, J=6.32 Hz, 3H) 1.52-1.70 (m, 2H) 3.17 (s, 3H) 3.26-3.36 (m, 3H) 7.72 (d, J=8.59 Hz, 2H) 8.07 (d, J=6.57 Hz, 2H) 8.27-8.50 (m, 2H) 8.61 (t, J=5.43 Hz, 2H) 8.76-8.96 (m, 1H) 13.46 (br. s., 1H). MS m/z [M+H]+ 392.1.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 3-methoxybutan-1-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.05 (d, J=6.32 Hz, 3H) 1.52-1.70 (m, 2H) 3.17 (s, 3H) 3.26-3.36 (m, 3H) 7.72 (d, J=8.59 Hz, 2H) 8.07 (d, J=6.57 Hz, 2H) 8.27-8.50 (m, 2H) 8.61 (t, J=5.43 Hz, 2H) 8.76-8.96 (m, 1H) 13.46 (br. s., 1H). MS m/z [M+H]+ 392.1.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 3-methoxybutan-1-amine 1H NMR (400 MHz, DMSO-d6) δ ppm 1.05 (d, J=6.32 Hz, 3 H) 1.52-1.70 (m, 2 H) 3.17 (s, 3 H) 3.26-3.36 (m, 3 H) 7.72 (d, J=8.59 Hz, 2 H) 8.07 (d, J=6.57 Hz, 2 H) 8.27-8.50 (m, 2H) 8.61 (t, J=5.43 Hz, 2 H) 8.76-8.96 (m, 1 H) 13.46 (br. s., 1 H). MS m/z [M+H]+ 392.1.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared in a manner similar to Example 112 using 6-(4-(4-cyanophenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and 3-methoxybutan-1-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.05 (d, J=6.32 Hz, 3H) 1.52-1.70 (m, 2H) 3.17 (s, 3H) 3.26-3.36 (m, 3H) 7.72 (d, J=8.59 Hz, 2H) 8.07 (d, J=6.57 Hz, 2H) 8.27-8.50 (m, 2H) 8.61 (t, J=5.43 Hz, 2H) 8.76-8.96 (m, 1H) 13.46 (br. s., 1H). MS m/z [M+H]+ 392.1.