HRID2284362

反应详情

EQUATION

反应方程式

HRID 2284362 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A microwave vial was charged with a mixture of 3-bromo-6-chloro-8-(4-methylpyridin-3-yl)imidazo[1,2-b]pyridazine (64 mg, 0.198 mmol), phenylboronic acid (24.12 mg, 0.198 mmol), tetrakis(triphenylphosphine)palladium(0) (22.86 mg, 0.020 mmol), dioxane (4 mL), and K3PO4 (0.297 mL, 0.593 mmol) (2.0 M water solution) was stirred at room temperature for 5 min. under nitrogen. The resulting mixture was heated to 100° C. for 8 h in microwave. The reaction mixture was cooled to room temperature, quenched with water, and diluted with EtOAc. The layers were separated and the aqueous layer was extracted with EtOAc (3×20 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by prep. HPLC to give 38 mg (44.3%) of the product. LC/MS: Rt=2.36 min. LC/MS (Condition A): 321.09/323.10.

WORKUP

后处理

  1. temperatureThe resulting mixture was heated to 100° C. for 8 h in microwave
  2. temperatureThe reaction mixture was cooled to room temperature
  3. customquenched with water
  4. additiondiluted with EtOAc
  5. customThe layers were separated
  6. extractionthe aqueous layer was extracted with EtOAc (3×20 mL)
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over anhydrous Na2SO4
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated under reduced pressure
  11. customThe residue was purified by prep