HRID42194

反应详情

EQUATION

反应方程式

HRID 42194 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
5 °C

PROCEDURE

实验过程

Methyltriphenylphosphonium iodide (115 mg, 0.28 mmol) is dissolved in THF (750 μL) and chilled to 5° C. While stirring add potassium t-butoxide (310 μL, 1M in THF, 0.31 mmol) to the solution. After 30 minutes add the mixture to a solution of 1-[4-(4-Benzyl-phthalazin-1-yl)-3,4,5,6-tetrahydro-2H-[1,2]bipyrazinyl-5′-yl]-ethanone (100 mg, 0.24 mmol) and THF (750 μL). Stir 30 minutes. Analysis shows 60-70% completion. A second portion of methyl triphenyl phosphonium iodide (115 mg, 0.28 mmol) is dissolved in THF (750 μl) and chilled to 5° C. While stirring add potassium t-butoxide (310 μL, 1M in THF, 0.31 mmol) to the solution. Again add this mixture to the current reaction. Reaction quickly proceeds to completion. Quench by adding saturated ammonium chloride. Concentrate in vacuo to remove THF and partition between water and EtOAc. Extract with EtOAc, and wash combined organics with brine. Concentrate EtOAc in vacuo. The residue is purified by flash chromatography on silica gel (EtOAc/Heptane) to afford the title compound (80 mg, 78%).

WORKUP

后处理

  1. stirringStir 30 minutes
  2. temperaturechilled to 5° C
  3. stirringWhile stirring
  4. additionAgain add this mixture
  5. customto the current reaction
  6. customReaction
  7. customQuench
  8. additionby adding saturated ammonium chloride
  9. concentrationConcentrate in vacuo
  10. customto remove THF
  11. custompartition between water and EtOAc
  12. extractionExtract with EtOAc
  13. washwash
  14. customThe residue is purified by flash chromatography on silica gel (EtOAc/Heptane)