反応式
[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3SCC)[N:8]([CH3:20])[C:5]2=[N:6][CH:7]=1.C(Cl)(Cl)Cl.Cl[C:26]1C=CC=C(C(OO)=O)[CH:27]=1.[S:36]([O-:40])([O-])(=[O:38])=S.[Na+].[Na+]>O>[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[S:36]([CH2:26][CH3:27])(=[O:40])=[O:38])[N:8]([CH3:20])[C:5]2=[N:6][CH:7]=1参加物
実験手順
To a mixture of 6-bromo-2-(2-ethylsulfanylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (0.20 g) and chloroform (3 ml), 3-chloroperbenzoic acid (purity: not less than 65%) (0.34 g) was added under ice-cooling, and then heated to room temperature, and stirred for 3.5 hours. Chloroform and saturated aqueous sodium thiosulfate solution were poured thereinto under ice-cooling, and stirred, and then, water was poured, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The resulting solid was washed with hexane, and dried to give 0.20 g of 6-bromo-2-(2-ethylsulfonylphenyl)-3-methyl-3H-imidazo[4,5-b]pyridine (hereinafter referred to as Present Compound 44).
後処理
- additionwas added under ice-
- temperaturecooling
- temperatureunder ice-cooling
- stirringstirred
- extractionextracted with ethyl acetate
- washThe organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- washThe resulting solid was washed with hexane
- customdried
出典と根拠
- ORDレコード
- ord-ddba5269e00c4fa9a96e7cb3ef2aa64b
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08853238B2
関連ノート
読み込み中…