反应 #40366

ord-7e6296a5515441d5b10b47b9b173f03f

反应方程式

CCN(C)c1nc(Oc2cc(C)c([N+](=O)[O-])cc2C)ncc1Cl
5-chloro-2-(2,5-dimethyl-4-nitrophenoxy)-N-ethyl-N-methylpyrimidin-4-amine
CO
methanol
CCN(C)c1nc(Oc2cc(C)c(N)cc2C)ncc1Cl
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. 1
    温度the mixture was refluxed for 4 h
  2. 2
    过滤was filtered by suction
  3. 3
    workup.ADDITIONEthyl acetate was added
  4. 4
    其他the organic layer was separated
  5. 5
    干燥dried over magnesium sulfate
  6. 6
    浓缩concentrated in vacuo and column chromatography (cyclohexane/ethyl acetate, 1:1)
  7. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07727986B2uspto-grants-2010_06