反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:12](=[O:17])[CH2:13][S:14]([CH3:16])=[O:15])=[C:6]([CH:11]=1)[N:7]([CH3:10])[CH:8]=O>COCCO>[F:1][C:2]1[CH:11]=[C:6]2[C:5]([C:12](=[O:17])[C:13]([S:14]([CH3:16])=[O:15])=[CH:8][N:7]2[CH3:10])=[CH:4][CH:3]=1参加物
3
実験手順
A solution of 5'-fluoro-N-methyl-2'-methylsulphinylacetylformanilide (0.77 g) in 2-methoxyethanol (25 ml) was heated to reflux over 20 minutes. After heating under reflux at 128° for 45 minutes the mixture was evaporated in vacuo to give 7-fluoro-1-methyl-3-methylsulphinyl-4-quinolone, m.p.225.5°-227° (0.69 g).
後処理
- temperatureto reflux over 20 minutes
- temperatureAfter heating
- temperatureunder reflux at 128° for 45 minutes the mixture
- customwas evaporated in vacuo
出典と根拠
- ORDレコード
- ord-6d07a6becd3e4270be25d4f2c5fdfd93
- 出典データセット
- uspto-grants-1991_04
- 特許番号
- US05011931
関連ノート
読み込み中…