反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
A stirred solution of 2-[[6-methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)-phenyl]-benzamide (Example 1; 3.98 g, 8.3 mmol) in dry toluene (200 mL) is purged with argon for 20 minutes at 25° C. Tributyl-1-propynylstannane (4.1 g of 80%, 9.96 mmol) and tetrakis(triphenylphosphine)palladium (0) (260 mg) are then added and the resulting mixture is heated at 100° C. for 17 hours under an argon atmosphere. The mixture is then cooled, treated with an aqueous solution of sodium hydroxide (85 mL of 0.1 M) and purged with air for 2 hours. The resulting mixture is extracted with EtOAc (3×100 mL). The organic phase is sequentially washed with water (2×40 mL) and saturated aqueous sodium chloride (1×40 mL), dried (Na2SO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent 33% EtOAc in hexane and recrystallised from diethylether-hexane to give the title compound as a pale-yellow crystalline solid; m.p. 123–124° C.
WORKUP
后处理
- temperatureThe mixture is then cooled
- custompurged with air for 2 hours
- extractionThe resulting mixture is extracted with EtOAc (3×100 mL)
- washThe organic phase is sequentially washed with water (2×40 mL) and saturated aqueous sodium chloride (1×40 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customthe solvent is evaporated under reduced pressure
- customto yield the crude product which
- customis purified by column chromatography on silica gel, eluent 33% EtOAc in hexane
- customrecrystallised from diethylether-hexane