反应 #40363

ord-83ad101b069c418abead533afb70f9d8

反应方程式

O
water
Cc1c(O)cccc1Cl
3-chloro-2-methyl-phenol
[H-].[Na+]
sodium hydride
Cc1cc(Oc2ccnc(Cl)n2)c(C)cc1N
4-(2-chloro-pyrimidin-4-yloxy)-2,5-dimethyl-phenylamine
Cc1cc(Oc2ccnc(Oc3cccc(Cl)c3C)n2)c(C)cc1N
4-[2-(3-chloro-2-methyl-phenoxy)-pyrimidin-4-yloxy]-2,5-dimethyl-phenylamine

溶剂

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    其他the organic layer was separated
  3. 3
    干燥dried over magnesium sulfate
  4. 4
    浓缩concentrated in vacuo, column chromatography (cycclhexane/ethyl acetate, 2:1)
  5. 5
    其他a second column chromatography (dichloromethane) yielded 640 mg (30%) with a purity of 85%

实验过程

A solution of 1.43 g (10 mmol) 3-chloro-2-methyl-phenol and 0.4 g sodium hydride (60% in paraffine, 10 mmol) in 20 ml THF were stirred for 30 min at ambient temperature. After adding 1.25 g (5 mmol) 4-(2-chloro-pyrimidin-4-yloxy)-2,5-dimethyl-phenylamine the mixture was stirred for 20 hrs at 60° C. After cooling down to ambient temperature 20 ml water was added and the organic layer was separated, dried over magnesium sulfate, concentrated in vacuo, column chromatography (cycclhexane/ethyl acetate, 2:1) and a second column chromatography (dichloromethane) yielded 640 mg (30%) with a purity of 85%; log P (pH=2.3)=2.81.

来源

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