HRID4942

反应详情

EQUATION

反应方程式

HRID 4942 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
140 °C

PROCEDURE

实验过程

1.67 g (0.011 mol) of 3-bromo-6-ethylpyridazine was added to 1.5 mL (10 mmol) ethyl isonipecotate and 3.5 mL (20 mmol) diisopropylethylamine and 5 mL N methylpyrrolidine (NMP). This mixture was heated to 140° C. for 4 hours. Upon cooling 100 mL of water was added to the mixture and the contents were extracted with methylene chloride then washed twice with water and once with brine and the solvent evaporated in vacuo. The resulting oil was eluted through a short silica gel plug with 80% ethyl acetate and 20% hexanes and dried in vacuo. This intermediate was taken up in 25 mL THF and was exposed to 3-fold excess lithium aluminum hydride with stirring under nitrogen for 1 hour. The reaction was chilled on ice and quenched by dropwise addition of water. The slurry was dried, treated with charcoal and filtered yielding 6-ethyl-3-(4-hydroxymethyl-1-piperidinyl)pyridazine (Formula IV: R1 =C2H5 ; Y=CH2 ).

WORKUP

后处理

  1. additionwas added to the mixture
  2. extractionthe contents were extracted with methylene chloride
  3. washthen washed twice with water and once with brine
  4. customthe solvent evaporated in vacuo
  5. washThe resulting oil was eluted through a short silica gel plug with 80% ethyl acetate and 20% hexanes
  6. customdried in vacuo
  7. temperatureThe reaction was chilled on ice
  8. customquenched by dropwise addition of water
  9. customThe slurry was dried
  10. additiontreated with charcoal
  11. filtrationfiltered