反应 #44518

ord-6c9f9b57843d4fe9a20c843dfd7e6fce

溶剂

反应条件

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

后处理

  1. 1
    萃取subjected to extraction with ethyl acetate
  2. 2
    workup.ADDITIONThen water was added
  3. 3
    萃取the mixture was subjected to extraction with ethyl acetate
  4. 4
    洗涤The organic layer was washed with water and brine sequentially
  5. 5
    干燥dried over anhydrous Na2SO4
  6. 6
    浓缩concentrated
  7. 7
    其他The resulting residue was purified by column chromatography

实验过程

6-(2-chloropyrimidin-4-yloxy)-N,2-dimethylbenzofuran-3-carboxamide (0.1 mmol) and 3-methoxyaniline (0.1 mmol) were dissolved in 0.5 ml DMF. To this was added p-TsOH monohydrate (0.2 mmol). The reaction mixture was stirred at 60° C. for 5 hours, and subjected to extraction with ethyl acetate. Then water was added and the mixture was subjected to extraction with ethyl acetate. The organic layer was washed with water and brine sequentially, dried over anhydrous Na2SO4, and concentrated. The resulting residue was purified by column chromatography to provide the title product in a yield of 80%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07737157B2uspto-grants-2010_06