HRID2381533

反应详情

EQUATION

反应方程式

HRID 2381533 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
25 °C

PROCEDURE

实验过程

A solution of 2-[4-(benzotriazol-1-yloxy)-6-oxo-6H-pyridazin-1-yl]-4-methyl-pentanoic acid [1-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-1H-pyrazol-3-yl]-amide (Example 109, Step 1, 0.25 g, 0.47 mmol) in acetonitrile (10 mL, 0.048M) was treated with cesium carbonate (0.31 g, 0.95 mmol) and 1H-indol-4-ol (75.4 mg, 0.56 mmol). The resulting reaction mixture was stirred at 25° C. for 3.5 h. At this time, the reaction was treated with N,N-dimethylformamide (1.0 mL) and the reaction was heated at 80° C. overnight. The reaction mixture was then concentrated in vacuo and partitioned between water (75 mL) and ethyl acetate (75 mL). The emulsified bilayer was filtered through filter paper and rinsed with water and ethyl acetate. The layers were separated, and the organics were washed with a saturated aqueous sodium chloride solution (50 mL). The combined aqueous layers were acidified with a 1N aqueous hydrochloric acid solution and extracted with ethyl acetate (50 mL). The combined organic layers were dried over magnesium sulfate, filtered, rinsed, and concentrated in vacuo. Silica gel column chromatography (AnaLogix 24 g, 1-10% methanol/methylene chloride) afforded 2-[4-(1H-indol-4-yloxy)-6-oxo-6H-pyridazin-1-yl]-4-methyl-pentanoic acid [1-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-1H-pyrazol-3-yl]-amide (207.1 mg, 81%) as a viscous brown/black oil as a mixture of diastereomers.

WORKUP

后处理

  1. customThe resulting reaction mixture
  2. temperaturethe reaction was heated at 80° C. overnight
  3. concentrationThe reaction mixture was then concentrated in vacuo
  4. custompartitioned between water (75 mL) and ethyl acetate (75 mL)
  5. filtrationThe emulsified bilayer was filtered
  6. filtrationthrough filter paper
  7. washrinsed with water and ethyl acetate
  8. customThe layers were separated
  9. washthe organics were washed with a saturated aqueous sodium chloride solution (50 mL)
  10. extractionextracted with ethyl acetate (50 mL)
  11. dry with materialThe combined organic layers were dried over magnesium sulfate
  12. filtrationfiltered
  13. washrinsed
  14. concentrationconcentrated in vacuo