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
PROCEDURE
实验过程
250 mg of 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 2), 8 mL of N,N-dimethylformamide, 7.7 mg of palladium acetate, 197 mg of cuprous iodide and 71.3 mg of 1,2,4-triazole are placed in a microwave tube. The reaction mixture is heated for 2.5 hours in a microwave machine set at 200° C. The cooled reaction mixture is filtered, the insoluble matter is rinsed with N,N-dimethylformamide, dichloromethane and methanol and the combined filtrates are concentrated to dryness under reduced pressure. The residue is chromatographed on a silica cartridge, eluting with a 90/10 mixture of dichloromethane and methanol. The fractions containing the pure expected product are combined and evaporated to dryness under reduced pressure to give 40 mg of N-phenyl-6-(1H-1,2,4-triazol-3-yl)imidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.
WORKUP
后处理
- temperatureThe reaction mixture is heated for 2.5 hours in a microwave machine
- customset at 200° C
- customThe cooled reaction mixture
- filtrationis filtered
- washthe insoluble matter is rinsed with N,N-dimethylformamide, dichloromethane and methanol
- concentrationthe combined filtrates are concentrated to dryness under reduced pressure
- customThe residue is chromatographed on a silica cartridge
- washeluting with a 90/10 mixture of dichloromethane and methanol
- additionThe fractions containing the pure expected product
- customevaporated to dryness under reduced pressure