HRID2270245

反应详情

EQUATION

反应方程式

HRID 2270245 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A solution of 3-benzyloxy-5,6,7,8-tetrafluoro-1H-quinazoline-2,4-dione (Example W-3, 0.90 g, 2.7 mmol), in DMA (10 mL) was reacted with pyrrolidine (0.55 mL, 6.6 mmol) and heated to 60° C. for 3 hours. The mixture was then cooled and quenched with H2O and acidified with citric acid. The mixture was then extracted with ethyl acetate, dried with MgSO4, and concentrated. The residue was triturated with diethyl ether/hexanes and the solid filtered and dried (0.87 g). A portion of the solid (0.500 g, 1.28 mmol) was dissolved in DMF and reacted with ethyl iodide (1.0 mL, 12.77 mmol) and sodium hydride (0.060 g, 1.5 mmol). The mixture was stirred for 16 hours. The mixture was quenched with H2O and extracted with ethyl acetate. The organic layers were combined, dried with sodium sulfate, and concentrated. The residue was triturated with diethyl ether and filtered to yield 0.25 g of the title compound as a solid.

WORKUP

后处理

  1. temperatureThe mixture was then cooled
  2. customquenched with H2O
  3. extractionThe mixture was then extracted with ethyl acetate
  4. dry with materialdried with MgSO4
  5. concentrationconcentrated
  6. customThe residue was triturated with diethyl ether/hexanes
  7. filtrationthe solid filtered
  8. customdried (0.87 g)
  9. customThe mixture was quenched with H2O
  10. extractionextracted with ethyl acetate
  11. dry with materialdried with sodium sulfate
  12. concentrationconcentrated
  13. customThe residue was triturated with diethyl ether
  14. filtrationfiltered