Piperidine → 7-Fluoro-3-hydroxy-1-methyl-4quinolone
反応式
C([O:9][C:10]1[C:19](=[O:20])[C:18]2[C:13](=[CH:14][C:15]([F:21])=[CH:16][CH:17]=2)[N:12]([CH3:22])[CH:11]=1)(=O)C1C=CC=CC=1.N1CCCCC1>ClCCl>[F:21][C:15]1[CH:14]=[C:13]2[C:18]([C:19](=[O:20])[C:10]([OH:9])=[CH:11][N:12]2[CH3:22])=[CH:17][CH:16]=1参加物
4
実験手順
A mixture of 7-fluoro-1-methyl-4-oxo-1,4-dihydro-quinol-3-yl benzoate (1 0 g), piperidine (3.7 ml) and dichloromethane (200 ml) was stirred at ambient temperature for 2 days under nitrogen. The solvent was removed by distillation at 50°. The resultant solid was triturated with diethyl ether 100 ml), collected and washed with diethyl ether (2×100 ml) to give the novel compound 7-fluoro-3-hydroxy-1 -methyl-4-quinolone, m.p. 283°-285°.
後処理
- customThe solvent was removed by distillation at 50°
- customThe resultant solid was triturated with diethyl ether 100 ml),
- customcollected
- washwashed with diethyl ether (2×100 ml)
出典と根拠
- ORDレコード
- ord-48b4e361caff423590e18d04a35832f5
- 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…