Sodium Hydroxide → HCID 22018411、化合物
反応式
C1(C(=[N:14][C:15]2[CH:16]=[C:17]3[C:22](=[CH:23][CH:24]=2)[CH:21]=[C:20]([C:25]([C:30]2[N:31]=[CH:32][N:33]([C:35]([C:48]4[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=4)([C:42]4[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=4)[C:36]4[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=4)[CH:34]=2)([OH:29])[CH:26]([CH3:28])[CH3:27])[CH:19]=[CH:18]3)C2C=CC=CC=2)C=CC=CC=1.C([O-])(=O)C.[Na+].Cl.NO.[OH-].[Na+]>C1COCC1.CO>[NH2:14][C:15]1[CH:16]=[C:17]2[C:22](=[CH:23][CH:24]=1)[CH:21]=[C:20]([C:25]([C:30]1[N:31]=[CH:32][N:33]([C:35]([C:48]3[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=3)([C:42]3[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=3)[C:36]3[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=3)[CH:34]=1)([OH:29])[CH:26]([CH3:28])[CH3:27])[CH:19]=[CH:18]2参加物
実験手順
1-{6-[(Diphenylmethylene)amino]naphthalen-2-yl}-2-methyl-1-(1-trityl-1H-imidazol-4-yl)-1-propanol (15.0 g) was dissolved in THF (5 ml)-methanol (5 ml) and sodium acetate (285 mg) and hydroxylamine hydrochloride (181 mg) were added. The mixture was stirred at room temperature for 20 min. 0.1N aqueous sodium hydroxide solution was added and the mixture was extracted with ethyl acetate, washed with saturated brine and dried to give a crude product of 1-(6-aminonaphthalen-2-yl)-2-methyl-1-(1-trityl-1H-imidazol-4-yl)-1-propanol as a pale-yellow oily substance. This product was dissolved in dichloromethane (100 ml), and pyridine (5.3 ml) and acetic anhydride (4.1 ml) were added. The mixture Was stirred at room temperature for 40 min. Saturated aqueous sodium hydrogen carbonate was added, and the mixture was extracted with dichloromethane and dried. The solvent was evaporated and the residue was recrystallized from ethyl acetate to give the title compound (11.6 g) as pale-red crystals.
後処理
- additionwere added
- extractionthe mixture was extracted with ethyl acetate
- washwashed with saturated brine
- customdried
出典と根拠
- ORDレコード
- ord-36f71b678be648a28eb184f299da1e85
- 出典データセット
- uspto-grants-2004_10
- 特許番号
- US06800778B1
反応ノート
読み込み中…