反応式
[Cl:1][C:2]1[C:9]([CH2:10][CH2:11][CH3:12])=[C:8](F)[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[NH2:14][C@@H:15]([C:19]([OH:21])=[O:20])[C@H:16]([CH3:18])[OH:17].C([O-])([O-])=O.[K+].[K+]>CS(C)=O>[Cl:1][C:2]1[C:9]([CH2:10][CH2:11][CH3:12])=[C:8]([NH:14][C@H:15]([C@@H:16]([OH:17])[CH3:18])[C:19]([OH:21])=[O:20])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]参加物
反応条件
- 温度
- 80 °C
実験手順
2-Chloro-4-fluoro-3-propylbenzonitrile (CAS 924626-89-1, 3.22 g, 16.3 mmol) was mixed together with H-D-Thr-OH (2.33 g, 19.6 mmol) in DMSO (30 mL) at room temperature. K2CO3 (4.73 g, 34.2 mmol) was added and the reaction mixture was stirred at 80° C. for 40 h. The reaction mixture was then cooled to room temperature and partitioned between water and EtOAc. The layers were separated and the aqueous extract was washed once with EtOAc. The aqueous extract was then acidified by slow addition of citric acid and stirred for 10 min at room temperature. The solution was extracted with EtOAc several times and the organic extracts were combined, washed with water, dried over Na2SO4, filtered, and concentrated in vacuo to obtain the crude product (0.650 g, 13% yield), which was carried on to the next step without further purification.
後処理
- temperatureThe reaction mixture was then cooled to room temperature
- custompartitioned between water and EtOAc
- customThe layers were separated
- extractionthe aqueous extract
- washwas washed once with EtOAc
- extractionThe aqueous extract
- additionwas then acidified by slow addition of citric acid
- stirringstirred for 10 min at room temperature
- extractionThe solution was extracted with EtOAc several times
- washwashed with water
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-4af266d120964e22a6f9080975d44983
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08642632B2
関連ノート
読み込み中…