反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([N:11]2[CH2:15][CH:14]([O:16][CH3:17])[CH2:13][NH:12]2)=[O:10])=[CH:4][CH:3]=1.[CH3:18][S:19]([C:22]1[N:27]=[C:26]([C:28](Cl)=[O:29])[CH:25]=[CH:24][N:23]=1)(=O)=O.[OH-].[Na+]>ClCCl.C(=O)([O-])[O-].[Na+].[Na+]>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([N:11]2[CH2:15][CH:14]([O:16][CH3:17])[CH2:13][N:12]2[C:28]([C:26]2[CH:25]=[CH:24][N:23]=[C:22]([S:19][CH3:18])[N:27]=2)=[O:29])=[O:10])=[CH:4][CH:3]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
2-(4-Fluorophenyl)-1-(4-methoxy-pyrazolidin-1-yl)-ethanone, 47, (7.67 g, 32.2 mmol) and 2-methylsulfonyl-pyrimidine-4-carbonyl chloride (9.11 g, 48.3 mmol) are dissolved in dichloromethane (150 mL). A 0.5 N aqueous solution of sodium hydroxide (150 mL) is added steadily via addition funnel and the mixture is stirred vigorously at room temperature for 4 hours. The reaction is diluted with 5% aqueous sodium carbonate solution (1 L). The mixture is extracted with dichloromethane (6×200 mL). The combined organic layers are dried over magnesium sulfate, filtered and concentrated to give a red oil. The crude material is purified by over silica (1:1 to 1:3 hexane/ethyl acetate to 100% ethyl acetate) to afford 10.3 g of the desired product as a brown, viscous oil.
後処理
- extractionThe mixture is extracted with dichloromethane (6×200 mL)
- dry with materialThe combined organic layers are dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a red oil
- customThe crude material is purified by over silica (1:1 to 1:3 hexane/ethyl acetate to 100% ethyl acetate)
出典と根拠
- ORDレコード
- ord-caa5a6d7ffe74d479029873264bd1763
- 出典データセット
- uspto-grants-2005_11
- 特許番号
- US06960593B2
関連ノート
読み込み中…