HRID385572

反应详情

EQUATION

反应方程式

HRID 385572 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

To a solution of 150 g of 2-chloro-5-fluoropyridin-3-amine in 600 mL of N,N-dimethylformamide, 190 mL of butyl acrylate and 287 mL of triethylamine were added under a nitrogen flow, and the mixture was stirred at 110° C. for 2 hours. The reaction mixture was cooled to 58° C., thereto were added 13.1 g of bis(tri-tert-butylphosphine)palladium(0), and the mixture was stirred at 110 to 120° C. for 40 minutes. The reaction mixture was cooled to 57° C., 13.1 g of bis(tri-tert-butylphosphine)palladium(0) was added thereto, and the mixture was stirred at 110 to 120° C. for 3 hours. The reaction mixture was cooled to room temperature, and water and ethyl acetate were added thereto. The insoluble substance was filtered off, the organic layer of the filtrate was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Cyclohexane and ethyl acetate were added to the resultant residue, and the solid was filtered off to obtain 200 g of butyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate as a light brown solid.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled to 58° C.
  2. stirringthe mixture was stirred at 110 to 120° C. for 40 minutes
  3. temperatureThe reaction mixture was cooled to 57° C.
  4. stirringthe mixture was stirred at 110 to 120° C. for 3 hours
  5. temperatureThe reaction mixture was cooled to room temperature
  6. filtrationThe insoluble substance was filtered off
  7. customthe organic layer of the filtrate was separated
  8. extractionthe aqueous layer was extracted with ethyl acetate
  9. washthe resultant solution was washed sequentially with water
  10. dry with materiala saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate
  11. distillationthe solvent was distilled off under reduced pressure
  12. additionCyclohexane and ethyl acetate were added to the resultant residue
  13. filtrationthe solid was filtered off