HRID1796944

反应详情

EQUATION

反应方程式

HRID 1796944 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

At 0° C., methanesulfonyl chloride (1.79 g, 15.64 mmol) is added to a solution of (5R)-5-(hydroxymethyl)-3-[4-(2-oxo-1-pyrrolidinyl)phenyl]-1,3-oxazolidin-2-one (3.6 g, 13.0 mmol) and triethylamine (2.9 g, 28.7 mmol) in dichloromethane (160 ml). The reaction mixture is stirred at 0° C. for 1.5 hours and at room temperature for 3 hours and then washed with water, and the aqueous phase is reextracted with dichloromethane. The combined organic phases are dried (magnesium sulfate), filtered and concentrated under reduced pressure. The residue (1.67 g) is then dissolved in acetonitrile (70 ml), phthalimide potassium (2.62 g, 14.16 mmol) is added and the mixture is stirred in a closed vessel in a microwave oven at 180° C. for 45 min. Insoluble residue is removed from the mixture by filtration, the filtrate is evaporated under reduced pressure, the residue (1.9 g) is dissolved in methanol and hydrazine hydrate (0.47 g, 9.37 mmol) is added. The reaction mixture is heated under reflux for 2 hours and cooled, saturated sodium bicarbonate solution is added and the mixture is extracted six times with methylene chloride (2 l in total). The combined organic phases are dried (magnesium sulfate), filtered and concentrated under reduced pressure.

WORKUP

后处理

  1. washwashed with water
  2. dry with materialThe combined organic phases are dried (magnesium sulfate)
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. dissolutionThe residue (1.67 g) is then dissolved in acetonitrile (70 ml)
  6. stirringthe mixture is stirred in a closed vessel in a microwave oven at 180° C. for 45 min
  7. customInsoluble residue is removed from the mixture by filtration
  8. customthe filtrate is evaporated under reduced pressure
  9. dissolutionthe residue (1.9 g) is dissolved in methanol
  10. temperatureThe reaction mixture is heated
  11. temperatureunder reflux for 2 hours
  12. temperaturecooled
  13. extractionthe mixture is extracted six times with methylene chloride (2 l in total)
  14. dry with materialThe combined organic phases are dried (magnesium sulfate)
  15. filtrationfiltered
  16. concentrationconcentrated under reduced pressure