HRID1097653

反应详情

EQUATION

反应方程式

HRID 1097653 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of 8-chloro-7-(2-propen-1-yl)-3-propyl-3,7-dihydro-1H-purine-2,6-dione (200 mg, 0.74 mmol) in THF (4 ml) was treated with 3-[3-(phenylmethyl)-1,2,4-oxadiazol-5-yl]-1-propanol (195 mg, 0.89 mmol) and PPh3 (254 mg, 0.96 mmol). DBAD (223 mg, 0.96 mmol) was added in one portion and the mixture was left to stir at rt under nitrogen for 18 h. The mixture was partitioned between EtOAc and 2M HCl (aq). The organic layer was separated, washed with brine, dried (MgSO4) and concentrated. The crude product was purified by a silica SPE column using a 0-70% cyclohexane/EtOAc gradient. The product fractions were combined, concentrated and further purified by a silica SPE column using a 0-60% cyclohexane/EtOAc gradient. The product fractions were combined and concentrated then dissolved in anhydrous THF (4 ml). The solution was degassed by high vacuum then Pd(PPh3)4 (86 mg, 0.074 mmol) and morpholine (644 μl, 7.4 mmol) were added and the mixture left to stir at rt under nitrogen for 1 day. The mixture was partitioned between EtOAc and HCl (aq). The organic layer was separated, washed with brine, dried (MgSO4) and concentrated by high vacuum. The crude product was purified by an aminopropyl SPE using MeOH to load the compound onto the column and wash through the impurities then a 2-4% AcOH/MeOH gradient to elute the product. The product fractions were combined and concentrated by high vacuum to leave the title compound as a white solid (74 mg, 23%).

WORKUP

后处理

  1. waitthe mixture was left
  2. customThe mixture was partitioned between EtOAc and 2M HCl (aq)
  3. customThe organic layer was separated
  4. washwashed with brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customThe crude product was purified by a silica SPE column
  8. concentrationconcentrated
  9. customfurther purified by a silica SPE column
  10. concentrationconcentrated
  11. dissolutionthen dissolved in anhydrous THF (4 ml)
  12. customThe solution was degassed by high vacuum
  13. waitthe mixture left
  14. stirringto stir at rt under nitrogen for 1 day
  15. customThe mixture was partitioned between EtOAc and HCl (aq)
  16. customThe organic layer was separated
  17. washwashed with brine
  18. dry with materialdried (MgSO4)
  19. concentrationconcentrated by high vacuum
  20. customThe crude product was purified by an aminopropyl SPE
  21. washwash through the impurities
  22. washa 2-4% AcOH/MeOH gradient to elute the product
  23. concentrationconcentrated by high vacuum