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
To 1-chloro-3-phenylisoquinoline (J. Het. Chem., 20, 1983, 121-128) (0.33 g, 1.37 mmol) in dry DMF (5 mL) was added 3-amino-5-methylpyrazole (0.27 g, 2.74 mmol) and potassium carbonate (0.57 g, 4.13 mmol)and the mixture was heated under reflux for 6 hours. The mixture was cooled and the bulk of DMF was evaporated. The residue was extracted twice with ethyl acetate and the combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated. The crude was purified by flash chromatography (SiO2, gradient DCM-MeOH) to give the title compound as a colourless oil; 1H NMR (MeOD) δ2.23 (3H, s), 5.61 (1H, s), 7.41 (1H, m), 7.52(2H, m), 7.62(1H, m), 7.81(1H, m), 8.07(1H, d), 8.19(2H, m), 8.29(1H, s), 8.54 (1H, d); MS 301.2 (M+H)+
WORKUP
后处理
- temperaturethe mixture was heated
- temperatureunder reflux for 6 hours
- temperatureThe mixture was cooled
- customthe bulk of DMF was evaporated
- extractionThe residue was extracted twice with ethyl acetate
- washthe combined organic layers were washed with brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customThe crude was purified by flash chromatography (SiO2, gradient DCM-MeOH)