Hydrochloric Acid → 4-(2-Oxo-2,3-dihydro-1H-imidazo[4,5-b]quinolin-7-yloxy)-butyric acid
反応式
[O:1]=[C:2]1[NH:22][C:5]2=[N:6][C:7]3[CH:8]=[CH:9][C:10]([O:14][CH2:15][CH2:16][CH2:17][C:18]([O:20]C)=[O:19])=[CH:11][C:12]=3[CH:13]=[C:4]2[NH:3]1.Cl>CO>[O:1]=[C:2]1[NH:22][C:5]2=[N:6][C:7]3[CH:8]=[CH:9][C:10]([O:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:11][C:12]=3[CH:13]=[C:4]2[NH:3]1参加物
4
実験手順
Methyl 4-[(2,3-dihydro-2-oxo-1H-imidazo[4,5-b]quinolin-7-yl)oxy]butanoate (1.0 g, 3.3 mmol) was added to a solution of 50% aqueous methanol containing 4N NaOH (2 mL). After stirring for 1 hour, the mixture was acidified to pH=3 by the addition of 2N HCl. The precipitate was washed with water, methanol and diethyl ether to give 4-[(2,3-dihydro-2-oxo-1H-imidazo[4,5-b]quinolin-7-yl)oxy]butyric acid as a partial hydrate (0.84 g, 88%). An analytical sample was prepared by crystalization from dimethylformamide/H2O and had m.p.>320°.
後処理
- washThe precipitate was washed with water, methanol and diethyl ether
出典と根拠
- ORDレコード
- ord-8df33cc007ce4e258390f5b7634aa8db
- 出典データセット
- uspto-grants-1988_10
- 特許番号
- US04775674
反応ノート
読み込み中…