HRID1359958

反应详情

EQUATION

反应方程式

HRID 1359958 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
4 °C

PROCEDURE

实验过程

2-(6-Bromopyridin-3-yl)ethanol (40 mg, 0.20 mmol) was dissolved in dichloroethane (3 ml), 200 mg of triethylamine was added to the solution, and the mixture was stirred at 4° C. under ice cooling. Mesyl chloride (68 mg, 0.60 mmol) was added to the reaction solution. After the dropwise addition, the mixture was stirred at 4° C. for 1 hr under ice cooling and was further stirred at room temperature for 30 min. The reaction solution was poured into 10 ml of iced water, was extracted with ml of ethyl acetate, and the extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under the reduced pressure. The residue was dissolved in DMF (2 ml), and the solution was stirred at room temperature. A 2 M solution (1 ml) of dimethylamine (2 mmol) in methanol was added thereto, and the mixture was stirred at 5.0° C. for 4 hr. The reaction solution was poured into 10 ml of iced water and was extracted with 20 ml of ethyl acetate. The extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under the reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate:methanol=10:1) to give 12 mg (yield 28.1%) of the title compound.

WORKUP

后处理

  1. additionAfter the dropwise addition
  2. stirringthe mixture was stirred at 4° C. for 1 hr under ice cooling
  3. stirringwas further stirred at room temperature for 30 min
  4. extractionwas extracted with ml of ethyl acetate
  5. dry with materialthe extract was dried over anhydrous sodium sulfate
  6. filtrationAfter filtration
  7. concentrationthe filtrate was concentrated under the reduced pressure
  8. dissolutionThe residue was dissolved in DMF (2 ml)
  9. stirringthe solution was stirred at room temperature
  10. stirringthe mixture was stirred at 5.0° C. for 4 hr
  11. extractionwas extracted with 20 ml of ethyl acetate
  12. dry with materialThe extract was dried over anhydrous sodium sulfate
  13. filtrationAfter filtration
  14. concentrationthe filtrate was concentrated under the reduced pressure
  15. customthe residue was purified by column chromatography on silica gel (ethyl acetate:methanol=10:1)