反应 #40366
ord-7e6296a5515441d5b10b47b9b173f03f
反应方程式
5-chloro-2-(2,5-dimethyl-4-nitrophenoxy)-N-ethyl-N-methylpyrimidin-4-amine
methanol
→
2-(4-amino-2,5-dimethylphenoxy)-5-chloro-N-ethyl-N-methylpyrimidin-4-amine
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度the mixture was refluxed for 4 h
- 2过滤was filtered by suction
- 3workup.ADDITIONEthyl acetate was added
- 4其他the organic layer was separated
- 5干燥dried over magnesium sulfate
- 6浓缩concentrated in vacuo and column chromatography (cyclohexane/ethyl acetate, 1:1)
- 7其他yielded 4.6 g (72%) with a purity of 96% log P (pH=2.3)=1.88
实验过程
To a solution of 8.86 g (20 mmol) 5-chloro-2-(2,5-dimethyl-4-nitrophenoxy)-N-ethyl-N-methylpyrimidin-4-amine in 50 ml hydrochloric acid and 50 ml methanol 13.5 g (60 mmol) tin-(II)-dichloro dihydrate was added and the mixture was refluxed for 4 h. After cooling down to ambient temperature the formed precipitate was filtered by suction, solved in water and brought to pH 8 with aqueous solution of sodium hydroxide. Ethyl acetate was added and the organic layer was separated, dried over magnesium sulfate, concentrated in vacuo and column chromatography (cyclohexane/ethyl acetate, 1:1) yielded 4.6 g (72%) with a purity of 96% log P (pH=2.3)=1.88.