Hydrochloric Acid → 1-(2-Cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)-4-((5-(trifluoromethyl)thiophen-2-yl)methoxy)pyridin-2(1H)-one hydrochloride
反応式
[ClH:1].[CH:2]1([C:5]2[N:6]=[C:7]3[CH:12]=[CH:11][C:10]([N:13]4[CH:18]=[CH:17][C:16]([O:19][CH2:20][C:21]5[S:22][C:23]([C:26]([F:29])([F:28])[F:27])=[CH:24][CH:25]=5)=[CH:15][C:14]4=[O:30])=[CH:9][N:8]3[C:31]=2[CH3:32])[CH2:4][CH2:3]1>CCOC(C)=O>[ClH:1].[CH:2]1([C:5]2[N:6]=[C:7]3[CH:12]=[CH:11][C:10]([N:13]4[CH:18]=[CH:17][C:16]([O:19][CH2:20][C:21]5[S:22][C:23]([C:26]([F:27])([F:28])[F:29])=[CH:24][CH:25]=5)=[CH:15][C:14]4=[O:30])=[CH:9][N:8]3[C:31]=2[CH3:32])[CH2:4][CH2:3]1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
4 M HCl in EtOAc (0.714 ml) was added to a solution of 1-(2-cyclopropyl-3-methylimidazo[1,2-a]pyridin-6-yl)-4-((5-(trifluoromethyl)thiophen-2-yl)methoxy)pyridin-2(1H)-one (1.27 g) in EtOAc (25 ml) at room temperature. The mixture was stirred at room temperature for 2 h. The resulting suspension was filtered and the precipitate was washed with EtOAc. The precipitate was crystallized from EtOH-IPE to give the title compound (0.39 g) as a white solid.
後処理
- filtrationThe resulting suspension was filtered
- washthe precipitate was washed with EtOAc
- customThe precipitate was crystallized from EtOH-IPE
出典と根拠
- ORDレコード
- ord-be8521d03e254778b42a13576311c83a
- 出典データセット
- uspto-grants-2016_06
- 特許番号
- US09365540B2
反応ノート
読み込み中…