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][C:17](=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19])[CH2:13][NH:12]2)=[O:10])=[CH:4][CH:3]=1.[CH3:23][S:24]([C:27]1[N:32]=[C:31]([C:33](Cl)=[O:34])[CH:30]=[CH:29][N:28]=1)(=O)=O.[OH-].[Na+]>ClCCl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([N:11]2[CH2:15][CH:14]([O:16][C:17](=[O:22])[C:18]([CH3:19])([CH3:21])[CH3:20])[CH2:13][N:12]2[C:33]([C:31]2[CH:30]=[CH:29][N:28]=[C:27]([S:24][CH3:23])[N:32]=2)=[O:34])=[O:10])=[CH:4][CH:3]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 2,2-dimethyl-propionic acid 1-[2-(4-fluorophenyl)acetyl]-pyrazolidin-4-yl ester, 32, (427 mg, 1.79 mmol) in dichloromethane (3 mL) is added 2-methylsulfonyl-pyrimidine-4-carbonyl chloride (676 mg, 3.58 mmol) followed by dropwise addition of a 1.0 N aqueous solution of sodium hydroxide (6 mL). The mixture is vigorously stirred at room temperature for 12 hours. The reaction is diluted with dichloromethane (25 mL) and washed with water (25 mL). The aqueous layer is back-extracted with dichloromethane (25 mL). The combined organic layers are washed with a saturated aqueous solution of sodium bicarbonate (25 mL) and brine (25 mL), dried, filtered and concentrated in vacuo. The resulting crude material is purified over silica (1:1 hexane/ethyl acetate to 100% ethyl acetate) to afford 464 mg (96.6% yield) of the desired product as a brown, viscous oil.
後処理
- washwashed with water (25 mL)
- extractionThe aqueous layer is back-extracted with dichloromethane (25 mL)
- washThe combined organic layers are washed with a saturated aqueous solution of sodium bicarbonate (25 mL) and brine (25 mL)
- customdried
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe resulting crude material is purified over silica (1:1 hexane/ethyl acetate to 100% ethyl acetate)
出典と根拠
- ORDレコード
- ord-9760ca086a3c45ccbfa35cf6a07cf08f
- 出典データセット
- uspto-grants-2004_05
- 特許番号
- US06730668B2
関連ノート
読み込み中…