HRID517890

反应详情

EQUATION

反应方程式

HRID 517890 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
150 °C

PROCEDURE

实验过程

A mixture of ethyl 7-(2-bromo-3-chloro-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoate (Intermediate EB) (150 mg, 0.371 mmol), 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (97 mg, 0.445 mmol) and potassium carbonate (154 mg, 1.112 mmol) were combined in a microwave vial. Dioxane (2 ml) was added and the flask was sealed and deoxygenated by evacuation/N2 purge (×3). Pd(Ph3P)4 (42.8 mg, 0.037 mmol) was added, the mixture was de-oxygenated by evacuation/N2 purge (×3) and heated at 150° C. for 3 hours using microwave radiation. The mixture was diluted with water and extracted with EtOAc (×2). The extracts were washed with brine, dried (MgSO4) and evaporated under reduced pressure to give a brown residue. The residue was purified by chromatography on silica eluting with 20-100% EtOAc in iso-hexane followed by 10% MeOH in DCM to afford ethyl 7-(3-chloro-2-(6-methylpyridin-3-yl)-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoate:

WORKUP

后处理

  1. customthe flask was sealed
  2. customdeoxygenated by evacuation/N2
  3. custompurge (×3)
  4. custompurge (×3)
  5. additionThe mixture was diluted with water
  6. extractionextracted with EtOAc (×2)
  7. washThe extracts were washed with brine
  8. dry with materialdried (MgSO4)
  9. customevaporated under reduced pressure
  10. customto give a brown residue
  11. customThe residue was purified by chromatography on silica eluting with 20-100% EtOAc in iso-hexane