Potassium Hydroxide → 1-amino-4-hydroxyquinolin-2(1H)-one
反応式
[OH-].[K+].[OH:3][C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]([N:14]=CC2C=CC=CC=2)[C:6](=[O:22])[C:5]=1C(OCC)=O>O1CCOCC1>[NH2:14][N:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:4]([OH:3])=[CH:5][C:6]1=[O:22]参加物
実験手順
To a solution of 25% by weight aqueous potassium hydroxide (200 mL) and 1,4-dioxane (50 mL) heated to 90-100° C. was added portion wise ethyl 4-hydroxy-2-oxo-1-{[phenylmethylene]amino}-1,2-dihydroquinoline-3-carboxylate (6.72 g, 20.0 mmol). The reaction mixture was heated at reflux for 90 minutes allowing distillation to occur and additional water and dioxane (30 mL each) were added to the reaction vessel to reach the original volume. The mixture was refluxed for an additional 90 minutes with distillation, cooled, washed with 200 mL of 1:1 diethyl ether/ethyl acetate, acidified with concentrated hydrochloric acid to pH 2 and the resulting solid was collected by filtration, washed with water and dried to constant mass to give 1-amino-4-hydroxyquinolin-2(1H)-one as a tan sold (3.22 g, 91% yield), MS (DCI) m/z 177 (M+H)+. 1H NMR (300 MHz, DMSO-d6) δ 5.56 (s, 2H) 5.94 (s, 1H) 7.20 (t, J=7.54 Hz, 1H) 7.62 (m, 1H) 7.85 (m, 2H) 11.33 (s, 1H).
後処理
- temperatureThe reaction mixture was heated
- temperatureat reflux for 90 minutes
- distillationdistillation
- additionadditional water and dioxane (30 mL each) were added to the reaction vessel
- temperatureThe mixture was refluxed for an additional 90 minutes with distillation
- temperaturecooled
- washwashed with 200 mL of 1:1 diethyl ether/ethyl acetate
- filtrationthe resulting solid was collected by filtration
- washwashed with water
- customdried to constant mass
出典と根拠
- ORDレコード
- ord-91069141cd1e4da8aae2b9ec128d86ed
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07662958B2
反応ノート
読み込み中…