HRID593979

反应详情

EQUATION

反应方程式

HRID 593979 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A slurry of 4-pyridylboronic acid (0.0950 g, 0.773 mmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride (0.0141 g, 0.0193 mmol), and N-(4-(5-iodopyrimidin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine (0.200 g, 0.387 mmol) and sodium carbonate 2.0 M in H2O (0.387 ml, 0.773 mmol) in 1.5 mL dioxane was flushed with nitrogen, sealed, and heated to 80° C. The reaction became dark and solids dissolved after 1 h. After 3 h, the reaction was judged complete. The reaction was cooled and diluted with DCM and water. The resulting aqueous emulsion was extracted 4×DCM. The combined organics were dried over anhyd sodium sulfate, filtered, and concentrated in vacuo. The material was adsorbed onto 1.8 g silica gel from MeOH/DCM, dried, and purified by silica gel chromatography (0-60-100% 90/10 DCM/MeOH in DCM) to give 4-phenyl-N-(4-(5-(pyridin-4-yl)pyrimidin-4-yloxy)phenyl)phthalazin-1-amine as a tan solid. MS m/z=469 [M+H]+. Calc'd for C29H20N6O: 468.5.

WORKUP

后处理

  1. customsealed
  2. dissolutionsolids dissolved after 1 h
  3. temperatureThe reaction was cooled
  4. extractionThe resulting aqueous emulsion was extracted 4×DCM
  5. dry with materialThe combined organics were dried over anhyd sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customdried
  9. custompurified by silica gel chromatography (0-60-100% 90/10 DCM/MeOH in DCM)