反応式
[F:1][C:2]1[C:11]([F:12])=[C:10]([F:13])[C:9]([F:14])=[C:8]2[C:3]=1[C:4](=[O:28])[C:5]([C:23]([O:25]CC)=[O:24])=[CH:6][N:7]2[C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][C:16]=1[F:22].S(=O)(=O)(O)O.C(O)(=O)C>O>[F:1][C:2]1[C:11]([F:12])=[C:10]([F:13])[C:9]([F:14])=[C:8]2[C:3]=1[C:4](=[O:28])[C:5]([C:23]([OH:25])=[O:24])=[CH:6][N:7]2[C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][C:16]=1[F:22]参加物
5
実験手順
40.1 g of ethyl 5,6,7,8-tetrafluoro-1-(2,4-difluorophenyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylate are added to a mixture of 28.5 ml of concentrated sulphuric acid, 250 ml of glacial acetic acid and 200 ml of water and the mixture is heated under reflux for 2 hours. The hot solution is poured onto ice and the precipitate is filtered off with suction, washed with water and dried. 34.5 g of the title compound of melting point 250°-252° C. are obtained.
後処理
- temperaturethe mixture is heated
- temperatureunder reflux for 2 hours
- additionThe hot solution is poured onto ice
- filtrationthe precipitate is filtered off with suction
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-c885914f5d934040a2c86a0595f3bafc
- 出典データセット
- uspto-grants-1991_02
- 特許番号
- US04990517
関連ノート
読み込み中…