HRID657080

反应详情

EQUATION

反应方程式

HRID 657080 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Crude 7-fluoro-1,5-naphthyridin-2(1H)-one 5-oxide (0.995 g, 5.524 mmol) and potassium carbonate were stirred in anhydrous DMF (20 mL) under argon, and allyl iodide (1.5 mL, ca. 3 eq.) was added. The mixture was stirred at rt overnight. The solvent was removed under reduced pressure and the residue was partitioned between DCM (100 mL) and water (50 mL). The organic phase was separated using a hydrophobic frit and the aqueous phase was extracted with DCM (2×50 mL). The combined organic extracts were dried over anhydrous sodium sulphate, filtered and evaporated under reduced pressure to give the crude product as a brown gum. This was purified by column chromatography on silica gel eluted with 0-10% methanol in DCM. Appropriate fractions were combined and evaporated under reduced pressure to give 7-fluoro-1-(2-propen-1-yl)-1,5-naphthyridin-2(1H)-one 5-oxide (0.341 g) as a tan amorphous solid.

WORKUP

后处理

  1. customThe solvent was removed under reduced pressure
  2. customthe residue was partitioned between DCM (100 mL) and water (50 mL)
  3. customThe organic phase was separated
  4. extractionthe aqueous phase was extracted with DCM (2×50 mL)
  5. dry with materialThe combined organic extracts were dried over anhydrous sodium sulphate
  6. filtrationfiltered
  7. customevaporated under reduced pressure
  8. customto give the crude product as a brown gum
  9. customThis was purified by column chromatography on silica gel
  10. washeluted with 0-10% methanol in DCM
  11. customevaporated under reduced pressure