HRID656150

反应详情

EQUATION

反应方程式

HRID 656150 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

3-(2,2-Dimethyl-1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamide (75 mg, 0.17 mmol), 1-[(5-bromo-2-thienyl)sulfonyl]pyrrolidine (60 mg, 0.17 mmol, 1 eq), PdCl2(dppf)-CH2Cl2 adduct (20 mg, 0.024 mmol, 0.15 eq), and potassium carbonate (100 mg, 0.72 mmol, 4.3 eq) were diluted in a mixture of 1,4-dioxane (3 mL) and water (1.5 mL) in a 2-5 mL microwave tube. The mixture was degassed by bubbling argon through for 5 minutes, then heated in a biotage microwave at 100° C. for 5 minutes. The crude reaction mixture was filtered through a thiol SPE cartridge (polymer labs) to remove palladium, and concentrated. The residue was dissolved in ˜3 mL of dmso, and filtered. The crude product was purified by ammonium hydroxide Gilson hplc, and the desired fractions were evaporated. The product was further purified by trituration from diethyl ether to afford 19.5 mg (21%) of the title compound.

WORKUP

后处理

  1. customThe mixture was degassed
  2. customby bubbling argon through for 5 minutes
  3. customThe crude reaction mixture
  4. filtrationwas filtered through a thiol SPE cartridge (polymer labs)
  5. customto remove palladium
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved in ˜3 mL of dmso
  8. filtrationfiltered
  9. customThe crude product was purified by ammonium hydroxide Gilson
  10. customthe desired fractions were evaporated
  11. customThe product was further purified by trituration from diethyl ether