HRID339675

反应详情

EQUATION

反应方程式

HRID 339675 的结构方程式

PROCEDURE

实验过程

To (E)-tert-butyl(1-(2-((2-(4-iodopyridin-2-yl)hydrazono)methyl)quinolin-8-yl)piperidin-4-yl)methylcarbamate (178 mg, 0.304 mmol) was added iodobenzene diacetate (IBD) (127 mg, 0.395 mmol). The reaction was stirred for 2 hours. Additional IBD (0.5 eq) was added and the reaction was stirred for another 2 hours and then quenched with saturated Na2S2O3 (5 mL). The organic layer was extracted with DCM, dried (Na2SO4) and concentrated. The crude material was purified by silica gel chromatography (EtOAc/Hexane/MeOH 2:1:0.1) to provide the final product.

WORKUP

后处理

  1. stirringthe reaction was stirred for another 2 hours
  2. customquenched with saturated Na2S2O3 (5 mL)
  3. extractionThe organic layer was extracted with DCM
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated
  6. customThe crude material was purified by silica gel chromatography (EtOAc/Hexane/MeOH 2:1:0.1)