HRID2360688

反应详情

EQUATION

反应方程式

HRID 2360688 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

To a mixture of 6-(4-hydroxy-phenyl)-3-methyl-1-(tetrahydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (215 mg), DIPEA (313 μL) and 1-benzyl-4-methyl-piperidin-4-ylamine (175 mg) in dichloroethane (7 mL), which was being stirred at 40° C., was added BEP (200 mg). The mixture was stirred at 40° C. for 60 min, then at r.t. overnight. Water was added and the mixture was extracted with dichloromethane. To the dichloromethane phase 30% sodium methoxide in methanol (0.4 mL) was added and stirred for 30 min. The mixture was filtered and the filtrate was washed with water, dried over magnesium sulfate and concentrated. The residue was chromatographed over silica (dichloromethane/methanol gradient) to give 1420 g (43%) of the title compound.

WORKUP

后处理

  1. additionwas added BEP (200 mg)
  2. stirringThe mixture was stirred at 40° C. for 60 min
  3. customat r.t.
  4. customovernight
  5. extractionthe mixture was extracted with dichloromethane
  6. additionTo the dichloromethane phase 30% sodium methoxide in methanol (0.4 mL) was added
  7. stirringstirred for 30 min
  8. filtrationThe mixture was filtered
  9. washthe filtrate was washed with water
  10. dry with materialdried over magnesium sulfate
  11. concentrationconcentrated
  12. customThe residue was chromatographed over silica (dichloromethane/methanol gradient)