反応式
[C:1]([N:4]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1)(=[O:3])[CH3:2].[F:10][C:11]1[CH:16]=[CH:15][C:14]([N:17]=[C:18]=[O:19])=[CH:13][CH:12]=1>O1CCCC1>[C:1]([N:4]1[CH2:9][CH2:8][N:7]([C:18](=[O:19])[NH:17][C:14]2[CH:15]=[CH:16][C:11]([F:10])=[CH:12][CH:13]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2]参加物
4
実験手順
To a stirred solution of 1-acetylpiperazine (0.648 g) in tetrahydrofuran (10 ml) was added 4-fluorophenyl isocyanate (0.574 g) at ambient temperature. After stirring at ambient temperature for 1 hour, the solvent was removed by evaporation under reduced pressure, and the residue was triturated with diisopropyl ether to give 1-acetyl-4-(4-fluorophenylcarbamoyl)piperazine (1.25 g).
後処理
- customthe solvent was removed by evaporation under reduced pressure
- customthe residue was triturated with diisopropyl ether
出典と根拠
- ORDレコード
- ord-f7241cc2bca64ba49d3504aa3103dea6
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06710043B1
関連ノート
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