HRID23553

反应详情

EQUATION

反应方程式

HRID 23553 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

Under a nitrogen atmosphere, 8-bromo-4-(4-isopropyloxycarbonyl-1,2,3,6-tetrahydropyridin-1-yl)-2-methylquinoline (5.9 g), 2,4-dichlorophenylboric acid (3.2 q) and sodium carbonate (4.8 g) were suspended in a mixed solvent of deaerated water (15 mL), toluene (7.5 mL) and ethanol (7.5 mL), followed by adding thereto tetrakis(triphenylphosphine)palladium (0.88 g), and the resulting mixture was heated under reflux for 5 hours. The reaction mixture was cooled to room temperature to be separated. After the aqueous phase was extracted with ethyl acetate, the combined organic phase was dried over anhydrous sodium sulfate. The desiccating agent was filtered off, after which the filtrate was concentrated under reduced pressure and the resultant residue was crystallized from diisopropyl ether. The crystals were collected by filtration and washed with a small amount of diisopropyl ether to obtain the title compound (5.3 g).

WORKUP

后处理

  1. additionby adding
  2. temperatureunder reflux for 5 hours
  3. customto be separated
  4. extractionAfter the aqueous phase was extracted with ethyl acetate
  5. dry with materialthe combined organic phase was dried over anhydrous sodium sulfate
  6. filtrationThe desiccating agent was filtered off
  7. concentrationafter which the filtrate was concentrated under reduced pressure
  8. customthe resultant residue was crystallized from diisopropyl ether
  9. filtrationThe crystals were collected by filtration
  10. washwashed with a small amount of diisopropyl ether