Trifluoroacetic acid → HCID 178426427、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[CH2:38][CH2:37][O:36][CH:35]([CH2:39][NH2:40])[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:40][CH2:39][CH:35]4[O:36][CH2:37][CH2:38][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 3922133(4-Methylmorpholin-2-yl)methanamine

HCID 178426451HCID 178426451、化合物

生成物 1

HCID 178426427HCID 178426427、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 (4-methylmorpholin-2-yl)methanamine 1H NMR (400 MHz, DMSO-d6) δ ppm 2.44 (s, 3 H) 2.78-2.94 (m, 4 H) 2.98-3.15 (m, 1 H) 3.31-3.58 (m, 4 H) 3.68 (t, J=11.75 Hz, 1 H) 3.78-3.95 (m, 1 H) 4.08 (dd, J=12.88, 3.03 Hz, 1 H) 7.67 (d, J=8.08 Hz, 1 H) 7.74 (s, 1 H) 7.78 (br. s., 1 H) 8.21 (d, J=6.32 Hz, 1 H) 8.44 (d, J=7.07 Hz, 2 H) 8.85-9.06 (m, 2 H) 9.93 (br. s., 1 H) 12.57-13.73 (m, 1 H). MS m/z [M+H]+ 433.2.