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
- 70 °C
PROCEDURE
实验过程
1.23 g of 4-(diphenylmethoxy)-1-piperidinepropanamine and 1.18 g of N-(6-chloroimidazo[1,2-b]pyridazine-2-carbonyl]-2,2-dimethylglycine ethyl ester were dissolved in 15 ml of N,N-dimethylformamide; 1.31 ml of N-ethyldiisopropylamine was added, followed by stirring at 70° C. for 9.5 hours. After cooling, aqueous sodium bicarbonate was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. The dry product was concentrated under reduced pressure; the residue was subjected to silica gel column chromatography and eluted with ethyl acetate:methanol:triethylamine (50:5:1). The desired fraction was collected, concentrated under reduced pressure and dissolved in 5 ml of ethyl acetate; 0.28 ml of a 4 N hydrogen chloride solution in ethyl acetate was added, followed by concentration again. Ethyl acetate was added to the residue; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 284 mg of the title compound.
WORKUP
后处理
- temperatureAfter cooling
- extractionfollowed by extraction with ethyl acetate
- washthe extract was washed with saturated saline
- dry with materialdried with magnesium sulfate
- concentrationThe dry product was concentrated under reduced pressure
- washeluted with ethyl acetate:methanol:triethylamine (50:5:1)
- customThe desired fraction was collected
- concentrationconcentrated under reduced pressure
- dissolutiondissolved in 5 ml of ethyl acetate
- addition0.28 ml of a 4 N hydrogen chloride solution in ethyl acetate was added
- concentrationfollowed by concentration again
- additionEthyl acetate was added to the residue
- customthe crystal precipitated
- filtrationwas collected by filtration
- washwashed with ethyl ether
- customdried