HRID1644505

反应详情

EQUATION

反应方程式

HRID 1644505 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of tert-butyl{1-[2-(6-chloro-1-oxido-3-oxo-1,2,4-benzotriazin-4(3H)-yl)ethyl]piperidin-4-yl}carbamate (Intermediate 206) (0.43 g) in acetic acid (8 mL) and water (2 mL) was added zinc dust (0.50 g). After 30 minutes, the solution was filtered and the filtrate concentrated. The residue was then treated with potassium ferricyanide (1.0 g) in water (20 mL). After 2 hours, the reaction was diluted with ethyl acetate. The aqueous layer was collected, the pH adjusted with solid Na2CO3 and extracted with ethyl acetate. The combined organic washes were dried (Na2SO4), filtered and concentrated. The residue was purified by chromatography on silica gel with 0-25% acetone in dichloromethane to yield 66 mg of the product.

WORKUP

后处理

  1. filtrationthe solution was filtered
  2. concentrationthe filtrate concentrated
  3. additionThe residue was then treated with potassium ferricyanide (1.0 g) in water (20 mL)
  4. waitAfter 2 hours
  5. additionthe reaction was diluted with ethyl acetate
  6. customThe aqueous layer was collected
  7. extractionextracted with ethyl acetate
  8. dry with materialThe combined organic washes were dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe residue was purified by chromatography on silica gel with 0-25% acetone in dichloromethane