HRID567681

反应详情

EQUATION

反应方程式

HRID 567681 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

3-Triisopropylsilyloxyanthranilic acid (0.8 g), 2,6-difluorobenzoyl chloride (0.71 mL) and triethyl amine/toluene (1/1) (25 mL) were reacted as described under (10). Reaction time 2 days. Extraction between ethyl acetate (100 mL) and HCl (1N,100 mL), followed by separation of the organic layer, drylng over MgSO4, filtering and evaporation gave a crude product which was dissolved in warm THF (20 mL) and precipitated with hexane. The resulting mixture was further purified on a silicagel column using dichloromethane as eluent. The isolated fraction (80 mg) was hydrolysed with 1% HCl in ethanol by stirring for 2 days at RT, and further hydrolysis after addition of HCl (4N, 5 mL) and ethyl acetate (10 mL). The organic layer was separated, evaporated and dried resulting in 2-(2,6-difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one (32 mg), mp.190-198. LC-MS showed the purity 86% with the corresponding O-triisopropylsilylated product as the impurity.

WORKUP

后处理

  1. customReaction time 2 days
  2. extractionExtraction between ethyl acetate (100 mL) and HCl (1N,100 mL)
  3. customfollowed by separation of the organic layer
  4. filtrationfiltering
  5. customevaporation
  6. customgave a crude product which
  7. customprecipitated with hexane
  8. customThe resulting mixture was further purified on a silicagel column
  9. customfurther hydrolysis
  10. customThe organic layer was separated
  11. customevaporated
  12. customdried
  13. customresulting in 2-(2,6-difluoro-phenyl)-8-hydroxy-benzo[d][1,3]oxazin-4-one (32 mg)