Tetrahydrofuran → HCID 178455216、化合物
反応式
[C:1](N1C=CN=C1)(N1C=CN=C1)=[O:2].[Si:13]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][NH:25][C:26]1[C:35]2[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=2)[N:29]=[C:28]([Cl:36])[C:27]=1[NH2:37])([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14].C1COCC1>N1C=CC=CC=1>[Si:13]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][N:25]1[C:26]2[C:35]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[N:29]=[C:28]([Cl:36])[C:27]=2[N:37]=[C:1]1[OH:2])([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]参加物
反応条件
- 温度
- 80 °C
実験手順
1,1′-Carbonyldiimidazole (32.6 g, 201 mmol) was added to a solution of N4-[4-(tert-butyldimethylsilanyloxy)butyl]-2-chloroquinoline-3,4-diamine (50.96 g, 134.1 mmol), THF (250 mL), and pyridine (250 mL), and the reaction was heated at 80° C. overnight and allowed to cool. The volatiles were removed under reduced pressure. The residue was dissolved in ethyl acetate (600 mL), and the resulting solution was washed sequentially with brine (2×400 mL) and water (2×400 mL) and then concentrated under reduced pressure. The resulting solid was triturated with diethyl ether (1 L), collected by filtration, washed with diethyl ether (800 mL), and dried under vacuum for 30 minutes to provide 28.39 g of 1-[4-(tert-butyldimethylsilanyloxy)butyl]-4-chloro-1H-imidazo[4,5-c]quinolin-2-ol as a white solid.
後処理
- temperatureto cool
- customThe volatiles were removed under reduced pressure
- dissolutionThe residue was dissolved in ethyl acetate (600 mL)
- washthe resulting solution was washed sequentially with brine (2×400 mL) and water (2×400 mL)
- concentrationconcentrated under reduced pressure
- customThe resulting solid was triturated with diethyl ether (1 L)
- filtrationcollected by filtration
- washwashed with diethyl ether (800 mL)
- customdried under vacuum for 30 minutes
出典と根拠
- ORDレコード
- ord-99d6db9956514dc59e779aefa9ad81ab
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08088790B2
反応ノート
読み込み中…