HRID527771

反应详情

EQUATION

反应方程式

HRID 527771 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

2-(Butyloxy)-8-(methyloxy)-9H-purin-6-amine trifluoroacetate (2 g, 5.69 mmol) and potassium carbonate (1.967 g, 14.23 mmol) were suspended in DMF (20 ml) and heated to 50° C., under nitrogen for 30 mins. The mixture was cooled to room temperature, 1-bromo-4-chlorobutane (0.656 ml, 5.69 mmol) was added and stirring continued at room temperature for 20 hours. The solvent was evaporated under reduced pressure and the residue was partitioned between DCM (40 ml) and water (40 ml). The layers were separated using a hydrophobic frit and the aqueous layer washed with DCM (10 ml). The combined organic extracts were concentrated in vacuo to give crude material that was purified by silica chromatography using the FlashMaster (70 g cartridge) eluting with a cyclohexane:ethyl acetate 0-100% gradient over 30 mins. The product-containing fractions were combined and evaporated to give the title compound as a white solid (1.4 g).

WORKUP

后处理

  1. temperatureThe mixture was cooled to room temperature
  2. customThe solvent was evaporated under reduced pressure
  3. customthe residue was partitioned between DCM (40 ml) and water (40 ml)
  4. customThe layers were separated
  5. washthe aqueous layer washed with DCM (10 ml)
  6. concentrationThe combined organic extracts were concentrated in vacuo
  7. customto give crude material that
  8. customwas purified by silica chromatography
  9. washeluting with a cyclohexane
  10. waitethyl acetate 0-100% gradient over 30 mins
  11. customevaporated