تفاعل #77543

ord-0c8d8f29888942789eda31322882c208

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthen cooled in ice bath
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for additional 4 hours
  3. 3
    أخرىThe 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
    تجفيفThe dichloromethane layer was dried over MgSO4
  6. 6
    ترشيحfiltered
  7. 7
    أخرىevaporated
  8. 8
    أخرىpurified by column chromatography (ethyl acetate:MeOH=10:1)

الإجراء التجريبي

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%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06706739B2uspto-grants-2004_03