6-Fluoropyridine-2-carboxaldehyde → (Z)-5-((2-(4-((((6-fluoropyridin-2-yl)methyl)amino)methyl)piperidin-1-yl)-6-methoxypyrimidin-4-yl)methylene)thiazolidine-2,4-dione
反応式
[NH2:1][CH2:2][CH:3]1[CH2:8][CH2:7][N:6]([C:9]2[N:14]=[C:13](/[CH:15]=[C:16]3/[C:17](=[O:22])[NH:18][C:19](=[O:21])[S:20]/3)[CH:12]=[C:11]([O:23][CH3:24])[N:10]=2)[CH2:5][CH2:4]1.[F:25][C:26]1[N:31]=[C:30]([CH:32]=O)[CH:29]=[CH:28][CH:27]=1>>[F:25][C:26]1[N:31]=[C:30]([CH2:32][NH:1][CH2:2][CH:3]2[CH2:8][CH2:7][N:6]([C:9]3[N:14]=[C:13](/[CH:15]=[C:16]4/[C:17](=[O:22])[NH:18][C:19](=[O:21])[S:20]/4)[CH:12]=[C:11]([O:23][CH3:24])[N:10]=3)[CH2:5][CH2:4]2)[CH:29]=[CH:28][CH:27]=1参加物
3
反応物 2
生成物 1
実験手順
(Z)-5-((2-(4-((((6-fluoropyridin-2-yl)methyl)amino)methyl)piperidin-1-yl)-6-methoxypyrimidin-4-yl)methylene)thiazolidine-2,4-dione was prepared using (Z)-5-((2-(4-(aminomethyl)piperidin-1-yl)-6-methoxypyrimidin-4-yl)methylene)thiazolidine-2,4-dione (Example 153), the general reductive amination procedure and 6-fluoropicolinaldehyde (26.1 mg, 59 mg theoretical, 43.9%). LC-MS m/z 459 (M+1).