HRID527772

反应详情

EQUATION

反应方程式

HRID 527772 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 1 hour. The mixture was cooled to room temperature, 1-bromo-5-chloropentane (0.75 ml, 5.69 mmol) was added and stirring was continued at room temperature for 18 hours. The reaction mixture was partitioned between DCM (40 ml) and water (40 ml) and the layers were separated using a hydrophobic frit. The aqueous layer was extracted again with DCM (10 ml) and the combined organics were washed with saturated lithium chloride solution, separated (hydrophobic frit) and concentrated in vacuo to give the title compound as a yellow oil (1.946 g).

WORKUP

后处理

  1. temperatureThe mixture was cooled to room temperature
  2. customThe reaction mixture was partitioned between DCM (40 ml) and water (40 ml)
  3. customthe layers were separated
  4. extractionThe aqueous layer was extracted again with DCM (10 ml)
  5. washthe combined organics were washed with saturated lithium chloride solution
  6. customseparated (hydrophobic frit)
  7. concentrationconcentrated in vacuo