2-Methyl-3-butyn-2-ol → [2-Chloro-4-(2,4-difluoro-phenylamino)-phenyl]-{5-[4-(1-hydroxy-1-methyl-ethyl)-[1,2,3]triazol-1-yl]-2-methyl-phenyl}-methanone
反応式
[N:1]([C:4]1[CH:5]=[CH:6][C:7]([CH3:28])=[C:8]([C:10]([C:12]2[CH:17]=[CH:16][C:15]([NH:18][C:19]3[CH:24]=[CH:23][C:22]([F:25])=[CH:21][C:20]=3[F:26])=[CH:14][C:13]=2[Cl:27])=[O:11])[CH:9]=1)=[N+:2]=[N-:3].[CH3:29][C:30]([OH:34])([C:32]#[CH:33])[CH3:31]>>[Cl:27][C:13]1[CH:14]=[C:15]([NH:18][C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][C:20]=2[F:26])[CH:16]=[CH:17][C:12]=1[C:10]([C:8]1[CH:9]=[C:4]([N:1]2[CH:33]=[C:32]([C:30]([OH:34])([CH3:31])[CH3:29])[N:3]=[N:2]2)[CH:5]=[CH:6][C:7]=1[CH3:28])=[O:11]参加物
3
実験手順
The reaction was carried out similarly as described in the preparation of compound 116, using compound 434 (0.125 mmol) and 2-methyl-but-3-yn-2-ol (0.125 mmol). The crude product was purified by continuous gradient flash chromatography using EtOAc/petroleum ether (40-60) 30:70 to 70:30 as the eluent to afford the title compound.
後処理
- customThe crude product was purified by continuous gradient flash chromatography