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 mixture of 6-chloro-7-cyclobutyl-3-phenyl-1,2,4-triazolo[4,3-b]pyridazine (144 mg, 0.52 mmol) and C-(1-methyl-1H-1,2,4-triazol-3-yl)methylamine hydrochloride (300 mg, 2.0 mmol) in triethylamine (1 ml) and dry DMF (1 ml) was stirred and heated at 100° C. in a sealed tube for 20 hours. Upon cooling the volatiles were removed in vacuo, and the residue was partitioned between dichloromethane and saturated aqueous sodium hydrogen carbonate. The aqueous was further extracted with dichloromethane (x2). The combined extracts were dried (Na2SO4), filtered and evaporated. The residue was purified by chromatograhy on silica gel, eluting with 2%→5%→10% methanol-dichloromethane to give, in order of elution:
WORKUP
后处理
- temperatureUpon cooling the volatiles
- customwere removed in vacuo
- customthe residue was partitioned between dichloromethane and saturated aqueous sodium hydrogen carbonate
- extractionThe aqueous was further extracted with dichloromethane (x2)
- dry with materialThe combined extracts were dried (Na2SO4)
- filtrationfiltered
- customevaporated
- customThe residue was purified by chromatograhy on silica gel
- washeluting with 2%→5%→10% methanol-dichloromethane
- customto give, in order of elution