{[1-(甲氧基甲基)环戊基]甲基}胺盐酸盐

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-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (1-(methoxymethyl)cyclopentyl)methanamine 1H NMR (400 MHz, DMSO-d6) δ ppm 1.26-1.38 (m, 2 H) 1.38-1.59 (m, 6 H) 2.37 (s, 3 H) 3.13 (s, 2 H) 3.21 (s, 3 H) 3.26 (d, J=6.32 Hz, 2 H) 7.59 (dd, J=7.83, 1.52 Hz, 1 H) 7.66 (s, 1 H) 7.73 (d, J=8.08 Hz, 1 H) 8.09 (s, 1 H) 8.33 (s, 2 H) 8.42 (t, J=6.06 Hz, 1 H) 8.82 (t, J=1.52 Hz, 1 H) 12.56-13.49 (m, 1 H). MS m/z [M+H]+ 446.2.

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-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (1-(methoxymethyl)cyclopentyl)methanamine. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.26-1.38 (m, 2H) 1.38-1.59 (m, 6H) 2.37 (s, 3H) 3.13 (s, 2H) 3.21 (s, 3H) 3.26 (d, J=6.32 Hz, 2H) 7.59 (dd, J=7.83, 1.52 Hz, 1H) 7.66 (s, 1H) 7.73 (d, J=8.08 Hz, 1H) 8.09 (s, 1H) 8.33 (s, 2H) 8.42 (t, J=6.06 Hz, 1H) 8.82 (t, J=1.52 Hz, 1H) 12.56-13.49 (m, 1H). MS m/z [M+H]+ 446.2.

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-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (1-(methoxymethyl)cyclopentyl)methanamine 1H NMR (400 MHz, DMSO-d6) δ ppm 1.26-1.38 (m, 2 H) 1.38-1.59 (m, 6 H) 2.37 (s, 3 H) 3.13 (s, 2 H) 3.21 (s, 3 H) 3.26 (d, J=6.32 Hz, 2 H) 7.59 (dd, J=7.83, 1.52 Hz, 1 H) 7.66 (s, 1 H) 7.73 (d, J=8.08 Hz, 1 H) 8.09 (s, 1 H) 8.33 (s, 2 H) 8.42 (t, J=6.06 Hz, 1 H) 8.82 (t, J=1.52 Hz, 1 H) 12.56-13.49 (m, 1 H). MS m/z [M+H]+ 446.2.

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-cyano-2-methylphenyl)-5-hydroxy-1H-pyrazol-1-yl)nicotinic acid and (1-(methoxymethyl)cyclopentyl)methanamine. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.26-1.38 (m, 2H) 1.38-1.59 (m, 6H) 2.37 (s, 3H) 3.13 (s, 2H) 3.21 (s, 3H) 3.26 (d, J=6.32 Hz, 2H) 7.59 (dd, J=7.83, 1.52 Hz, 1H) 7.66 (s, 1H) 7.73 (d, J=8.08 Hz, 1H) 8.09 (s, 1H) 8.33 (s, 2H) 8.42 (t, J=6.06 Hz, 1H) 8.82 (t, J=1.52 Hz, 1H) 12.56-13.49 (m, 1H). MS m/z [M+H]+ 446.2.