Реакция #70964

Уравнение реакции

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

Растворители

DMF

Условия реакции

Обработка

1. 1
   Температураheated at 80° C. overnight
2. 2
   ТемператураThen the reaction mixture was cooled to ambient temperature
3. 3
   Другоеquenched with methanol (4 ml)
4. 4
   ДругоеAfter evaporation of the solvent in vacuo, water (25 ml)
5. 5
   workup.ADDITIONwas added to the residue
6. 6
   Экстракцияthe mixture was extracted with dichloromethane (2×25 ml)
7. 7
   СушкаThe combined organic phases were dried over anhydrous MgSO4
8. 8
   ДругоеThe solvent was evaporated in vacuo
9. 9
   Другоеthe residue was purified by column chromatography with a mixture of chloroform:ethyl acetate (10:1) as the eluent

Методика

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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