Reaktion #77543

Reaktionsgleichung

1-Bromo-4-[(7-bromoheptyl)oxy] benzene

1-(2-chloro-4-pyridyl)-2-imidazolidinone

NaH

→

Compound 8

1-[7-(4-bromophenoxy)heptyl]-3-(2-chloro-4-pyridyl)-2-imidazolidinone

Lösungsmittel

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthen cooled in ice bath
2. 2
   workup.STIRRINGthe mixture was stirred at room temperature for additional 4 hours
3. 3
   SonstigeThe reaction was quenched with MeOH
4. 4
   workup.ADDITIONA saturated aqueous NH4Cl solution (5 mL) and dichloromethane (10 mL) were added to the residue
5. 5
   TrocknenThe dichloromethane layer was dried over MgSO4
6. 6
   Filtrationfiltered
7. 7
   Sonstigeevaporated
8. 8
   Sonstigepurified by column chromatography (ethyl acetate:MeOH=10:1)

Vorschrift

To a solution of 1-(2-chloro-4-pyridyl)-2-imidazolidinone (0.12 g, 0.63 mmol) dissolved in 10 mL dimethylformamide at 0° C. was added NaH (60% dispersion in mineral oil, 27.7 mg, 0.69 mmol). The mixture was stirred at room temperature for 30 minutes; then cooled in ice bath. 1-Bromo-4-[(7-bromoheptyl)oxy] benzene (0.22 g, 0.63 mmol) was added, and the mixture was stirred at room temperature for additional 4 hours. The reaction was quenched with MeOH, and the solvents were pumped off. A saturated aqueous NH4Cl solution (5 mL) and dichloromethane (10 mL) were added to the residue. The dichloromethane layer was dried over MgSO4, filtered, evaporated, and purified by column chromatography (ethyl acetate:MeOH=10:1) to give the product (i.e., Compound 8) as a white solid (0.19 g, 64%).

Quelle