Potassium Hydroxide → Brequinar Analog
反応式
[CH3:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:7][CH:6]=1)=O.[F:17][C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][CH:26]=1)[NH:23][C:22](=[O:27])[C:21]2=O.[OH-:29].[K+]>C(O)C.O>[C:8]1([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:7]=[CH:6][C:5]([C:3]2[C:2]([CH3:1])=[C:21]([C:22]([OH:27])=[O:29])[C:20]3[C:24](=[CH:25][CH:26]=[C:18]([F:17])[CH:19]=3)[N:23]=2)=[CH:10][CH:9]=1参加物
6
実験手順
4-Phenylpropiophenone (18.9 g, 0.09 mole) and 5-fluoroisatin (20 g, 0.09 mole) were suspended in 360 ml of ethanol and stirred mechanically as a solution of 35.2 g KOH in 100 ml water was added dropwise over 15 minutes. The reaction mixture was heated at reflux for 12 hours, cooled, and the ethanol evaporated under reduced pressure. The resulting yellow solid was dissolved in water and washed with ethyl ether. The aqueous layer was cooled to 5° and acidified with glacial acetic acid. The resulting yellow precipitate was filtered and dried. Recrystallization from 200 ml of dimethylformamide and 25 ml water provided 13.8 g of 2-(4-biphenylyl)-6-fluoro-3-methylquinoline-4-carboxylic acid as a white solid, m.p. 303°-306° (d).
後処理
- additionwas added dropwise over 15 minutes
- temperatureThe reaction mixture was heated
- temperatureat reflux for 12 hours
- temperaturecooled
- customthe ethanol evaporated under reduced pressure
- dissolutionThe resulting yellow solid was dissolved in water
- washwashed with ethyl ether
- temperatureThe aqueous layer was cooled to 5°
- filtrationThe resulting yellow precipitate was filtered
- customdried
- customRecrystallization from 200 ml of dimethylformamide and 25 ml water
出典と根拠
- ORDレコード
- ord-39e8c1b76a344f46965b0b8d11cf45ec
- 出典データセット
- uspto-grants-1991_07
- 特許番号
- US05032597
反応ノート
読み込み中…