Piperidine → 6-Fluoro-3-hydroxy-1-methyl-4-quinolone
反応式
C([O:9][C:10]1[C:19](=[O:20])[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([F:21])[CH:17]=2)[N:12]([CH3:22])[CH:11]=1)(=O)C1C=CC=CC=1.N1CCCCC1>ClCCl>[F:21][C:16]1[CH:17]=[C:18]2[C:13](=[CH:14][CH:15]=1)[N:12]([CH3:22])[CH:11]=[C:10]([OH:9])[C:19]2=[O:20]参加物
4
実験手順
A mixture of 6-fluoro-1 -methyl-4-oxo-1 ,4-dihydro-quinol-3-yl benzoate (1.90 g), piperidine (0.9 ml) and dry dichloromethane (50 ml) was stirred under nitrogen for 24 hours at ambient temperature. The solvent was removed by distillation and the residue triturated with diethyl ether (100 ml). The resultant solid was collected by filtration to give the novel compound 6-fluoro-3-hydroxy-1-methyl-4-quinolone, m.pp. 104°-106°.
後処理
- customThe solvent was removed by distillation
- customthe residue triturated with diethyl ether (100 ml)
- filtrationThe resultant solid was collected by filtration
出典と根拠
- ORDレコード
- ord-21bd8084f693488d94d2a08d4c529084
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US04997840
反応ノート
読み込み中…