Trifluoroacetic acid → HCID 178426423、化合物

反応式

C(O)(C(F)(F)F)=O.[C:8]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:17]=[N:18][N:19]([C:22]3[CH:30]=[CH:29][C:25]([C:26]([OH:28])=O)=[CH:24][N:23]=3)[C:20]=2[OH:21])=[C:12]([CH3:31])[CH:11]=1)#[N:9].[CH3:32][N:33]1[CH2:37][CH2:36][CH:35]([CH2:38][NH2:39])[CH2:34]1>>[C:8]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:17]=[N:18][N:19]([C:22]3[CH:30]=[CH:29][C:25]([C:26]([NH:39][CH2:38][CH:35]4[CH2:36][CH2:37][N:33]([CH3:32])[CH2:34]4)=[O:28])=[CH:24][N:23]=3)[C:20]=2[OH:21])=[C:12]([CH3:31])[CH:11]=1)#[N:9]

参加物

反応物 3

HCID 6422Trifluoroacetic acid

HCID 17389965(1-Methylpyrrolidin-3-yl)methanamine

HCID 178426451HCID 178426451、化合物

生成物 1

HCID 178426423HCID 178426423、化合物

実験手順

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.