反応式
[H-].[Na+].[F:3][C:4]1[C:13]([N+:14]([O-:16])=[O:15])=[CH:12][C:7]2[NH:8][C:9](=[O:11])[S:10][C:6]=2[CH:5]=1.Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20].O>CN(C)C=O>[CH2:22]([O:21][C:19]([CH2:18][N:8]1[C:7]2[CH:12]=[C:13]([N+:14]([O-:16])=[O:15])[C:4]([F:3])=[CH:5][C:6]=2[S:10][C:9]1=[O:11])=[O:20])[CH3:23]参加物
反応条件
- 温度
- 0 °C
実験手順
50% Oily sodium hydride (0.21 g) was suspended in N,N-dimethylformamide (5 ml), and the resultant suspension was cooled to 0° C. 6-Fluoro-5-nitro-2-(3H)-benzothiazolone (1.0 g) was portionwise added thereto at 0° C., and the mixture was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (0.86 g) was added to the reaction mixture at 0° C., and the temperature was gradually elevated to a temperature of 50° to 60° C., followed by stirring at that temperature for 3 hours. Water was added to the mixture, which was extracted with ethyl acetate. The extract was washed with water, dried and concentrated. The residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and toluene (1:9) to give 0.35 g of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone. m.p., 139.0°-140.0° C.
後処理
- customwas gradually elevated to a temperature of 50° to 60° C.
- stirringby stirring at that temperature for 3 hours
- extractionwas extracted with ethyl acetate
- washThe extract was washed with water
- customdried
- concentrationconcentrated
- customThe residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and toluene (1:9)
出典と根拠
- ORDレコード
- ord-e1055059a7c043b2ad5c3a511a43bac4
- 出典データセット
- uspto-grants-1988_01
- 特許番号
- US04720297
関連ノート
読み込み中…