反应 #70964

反应方程式

5-bromo-1,3-benzodioxole-4-carbaldehyde oxime

1-(2-chloroethyl)pyrrolidine hydrochloride

NaH

→

1-(5-bromo-1,3-benzodioxol-4-yl)-N-[2-(pyrrolidin-1-yl)ethoxy]methanimine

溶剂

DMF

反应条件

后处理

1. 1
   温度heated at 80° C. overnight
2. 2
   温度Then the reaction mixture was cooled to ambient temperature
3. 3
   其他quenched with methanol (4 ml)
4. 4
   其他After evaporation of the solvent in vacuo, water (25 ml)
5. 5
   workup.ADDITIONwas added to the residue
6. 6
   萃取the mixture was extracted with dichloromethane (2×25 ml)
7. 7
   干燥The combined organic phases were dried over anhydrous MgSO4
8. 8
   其他The solvent was evaporated in vacuo
9. 9
   其他the residue was purified by column chromatography with a mixture of chloroform:ethyl acetate (10:1) as the eluent

实验过程

To a stirred solution of 5-bromo-1,3-benzodioxole-4-carbaldehyde oxime (0.244 g, 1 mmol) in dry DMF (15 ml), 1-(2-chloroethyl)pyrrolidine hydrochloride (0.207 g, 1.22 mmol) and NaH (0.138 g, 3.45 mmol, 60% dispersion in oil) were added. The reaction mixture was stirred at ambient temperature for 5 minutes and then heated at 80° C. overnight. Then the reaction mixture was cooled to ambient temperature and quenched with methanol (4 ml). After evaporation of the solvent in vacuo, water (25 ml) was added to the residue, and the mixture was extracted with dichloromethane (2×25 ml). The combined organic phases were dried over anhydrous MgSO4. The solvent was evaporated in vacuo, and the residue was purified by column chromatography with a mixture of chloroform:ethyl acetate (10:1) as the eluent. After the isolation of the unreacted starting material, the eluent was changed to ethyl acetate:isopropanol:cc. NH3 (9:1:0.5). The crude product was digerated with water.

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