HRID896083

反应详情

EQUATION

反应方程式

HRID 896083 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

Dimethyl-((E)-3-tributylstannanyl-allyl)-amine (213 mg, 0.57 mmol) and (5-bromo-2-methoxy-phenyl)-[4-(2,4-difluoro-phenylamino)-phenyl]-methanone (200 mg, 0.475 mmol) are added to a solution of Pd(OAc)2 (10 mg, 0.047 mmol) and PPh3 (50 mg, 0.19 mmol) in diethylene glycol dimethyl ether (12 ml) and heated to 135 C under argon for 30 minutes. The reaction mixture is evaporated to dryness and purified via chromatography (SiO2, acetone/hexanes 6/4>1/0 followed by TBME/MeOH/NH3conc 100/0/0>90/10/1) to yield the crude product, which is dissolved in 2N HCl, washed with TBME and the aqueous phase made alkaline with saturated Na2CO3. Extraction with EtOAc and evaporation of the organic phase delivers the title compound, which was dissolved in acetone and filtered through a bed of SiO2 to give the desired product as yellow foam (55 mg; 28%).

WORKUP

后处理

  1. temperatureheated to 135 C under argon for 30 minutes
  2. customThe reaction mixture is evaporated to dryness
  3. custompurified via chromatography (SiO2, acetone/hexanes 6/4>1/0 followed by TBME/MeOH/NH3conc 100/0/0>90/10/1)
  4. customto yield the crude product, which
  5. washwashed with TBME
  6. extractionExtraction
  7. customwith EtOAc and evaporation of the organic phase
  8. dissolutionwas dissolved in acetone
  9. filtrationfiltered through a bed of SiO2