Water → (6-Chloro-5-nitro-pyrimidin-4-yloxy)-acetic acid methyl ester
反応式
[C:1]([O:5][CH3:6])(=[O:4])[CH2:2][OH:3].[H-].[Na+].[Cl:9][C:10]1[C:15]([N+:16]([O-:18])=[O:17])=[C:14](Cl)[N:13]=[CH:12][N:11]=1.O>CN(C)C=O>[CH3:6][O:5][C:1](=[O:4])[CH2:2][O:3][C:14]1[C:15]([N+:16]([O-:18])=[O:17])=[C:10]([Cl:9])[N:11]=[CH:12][N:13]=1参加物
実験手順
In a 50 ml flask at low temperature, methyl glycolate (0.22 ml, 2.8 mmol) and sodium hydride (114 mg, 2.8 mmol) were dissolved in N,N-dimethyl formamide (7 ml) and then stirred for 10 minutes. 4,6-dichloro-5-nitro-pyrimidine (500 mg, 2.6 mmol) dissolved in N,N-dimethyl formamide (6.5 ml) was added thereto dropwise and then stirred at the same temperature for additional 10 minutes, and then the temperature was raised to room temperature and stirred for additional 10 hours. After completion of the reaction by adding water, the mixture was extracted with dichloromethane, and the combined organic layer was washed with saturated saline solution, dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography eluting with a solvent of dichloromethane to obtain yellow liquid (280 mg, 44%).
後処理
- additionwas added
- stirringdropwise and then stirred at the same temperature for additional 10 minutes
- stirringstirred for additional 10 hours
- customAfter completion of the reaction
- extractionthe mixture was extracted with dichloromethane
- washthe combined organic layer was washed with saturated saline solution
- dry with materialdried over anhydrous sodium sulfate (Na2SO4)
- filtrationfiltered
- customevaporated under reduced pressure
- customThe residue was purified by column chromatography
- washeluting with a solvent of dichloromethane
出典と根拠
- ORDレコード
- ord-a2eeefe68afa40be80af4826e12eba4f
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08394792B2
反応ノート
読み込み中…