Potassium Carbonate → N-((1,3-dioxolan-2-yl)methyl)-3-methoxy-4-(2-(pyrrolidin-1-yl)ethoxy)aniline
反応式
C([O-])([O-])=O.[K+].[K+].Br[CH2:8][CH:9]1[O:13][CH2:12][CH2:11][O:10]1.[CH3:14][O:15][C:16]1[CH:17]=[C:18]([NH2:30])[CH:19]=[CH:20][C:21]=1[O:22][CH2:23][CH2:24][N:25]1[CH2:29][CH2:28][CH2:27][CH2:26]1>CS(C)=O>[O:10]1[CH2:11][CH2:12][O:13][CH:9]1[CH2:8][NH:30][C:18]1[CH:19]=[CH:20][C:21]([O:22][CH2:23][CH2:24][N:25]2[CH2:26][CH2:27][CH2:28][CH2:29]2)=[C:16]([O:15][CH3:14])[CH:17]=1参加物
5
反応条件
- 温度
- 80 °C
実験手順
A suspension of K2CO3 (235 mg, 1.70 mmol), 2-(bromomethyl)-1,3-dioxolane (400 mg, 1.70 mmol), and 3-methoxy-4-(2-(pyrrolidin-1-yl)ethoxy)benzenamine (3.0 g, 14.5 mmol), preparation described in PCT application WO 2002/101146, in DMSO (17 mL) was heated at 80° C. for 24 hr. After removal of any precipitate by filtration, the filtrate was partitioned between EtOAc/H2O (100/20 mL). The organic layer was washed with brine and dried over MgSO4. After removal of the solvent under vacuum, the residue was chromatographed on silica gel using 0%-20% gradient EtOAc/Hexanes to elute the title compound as a yellow brownish oil (150 mg, 27%) MS (ESI) 323 (M+H)+.
後処理
- customAfter removal of any precipitate
- filtrationby filtration
- customthe filtrate was partitioned between EtOAc/H2O (100/20 mL)
- washThe organic layer was washed with brine
- dry with materialdried over MgSO4
- customAfter removal of the solvent under vacuum
- customthe residue was chromatographed on silica gel using 0%-20% gradient EtOAc/Hexanes
- washto elute the title compound as a yellow brownish oil (150 mg, 27%)
出典と根拠
- ORDレコード
- ord-b952f422ff994537a25351a760b6689d
- 出典データセット
- uspto-grants-2011_06
- 特許番号
- US07956049B2
反応ノート
読み込み中…