HRID25147

反应详情

EQUATION

反应方程式

HRID 25147 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of 3,4-dihydro-2H-benzo[1,4]oxazin-6-yl amine (0.56 g, 3.73 mmol) in toluene (20 mL) was added ethyl 4,4,4-trifluoroacetoacetate (0.55 mL, 3.73 mmol) and 4 drops of pyridine. The solution was heated to reflux for 6 hours, then allowed to stir overnight at room temperature. The solvent was removed under vacuum and the residue triturated with diethyl ether. The solid was filtered off and washed with diethyl ether to yield a gray solid which was determined by 1HNMR to contain crude N-(3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,4,4-trifluoro-3-oxo-butyramide. The rest of the material in the filtrate was also determined by 1HNMR to be crude N-(3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,4,4-trifluoro-3-oxo-butyramide, but much less pure than the gray solid filtered off. The mixture was recovered by evaporating the ether. This mixture (0.8 g) was stirred in of concentrated sulfuric acid (8 mL) overnight at room temperature. The reaction mixture was then poured onto ice and neutralized by adding 1N sodium carbonate. The resulting solution was extracted three times with ethyl acetate, the extracts dried over magnesium sulfate, filtered and evaporated under vacuum to yield a brown oil. The brown oil (crude material) was purified by column chromatography on a Biotage system eluting with 4% methanol/ethyl acetate to yield 8-trifluoromethyl-3,4-dihydro-2H,5H-1-oxa-4,5diaza-anthracen-6-one as the main product.

WORKUP

后处理

  1. temperatureThe solution was heated
  2. temperatureto reflux for 6 hours
  3. customThe solvent was removed under vacuum
  4. customthe residue triturated with diethyl ether
  5. filtrationThe solid was filtered off
  6. washwashed with diethyl ether
  7. customto yield a gray solid which
  8. filtrationmuch less pure than the gray solid filtered off
  9. customThe mixture was recovered
  10. customby evaporating the ether
  11. stirringThis mixture (0.8 g) was stirred in of concentrated sulfuric acid (8 mL) overnight at room temperature
  12. additionThe reaction mixture was then poured onto ice
  13. additionby adding 1N sodium carbonate
  14. extractionThe resulting solution was extracted three times with ethyl acetate
  15. dry with materialthe extracts dried over magnesium sulfate
  16. filtrationfiltered
  17. customevaporated under vacuum
  18. customto yield a brown oil
  19. customThe brown oil (crude material) was purified by column chromatography on a Biotage system
  20. washeluting with 4% methanol/ethyl acetate