Реакция #6201

ord-a5c3cce7cb3a4ad4bf8f878f0513c956

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooling
  2. 2
    workup.STIRRINGthe mixture was stirred for at room temperature for 30 minutes
  3. 3
    ПромывкаThe reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water
  4. 4
    Другоеdried
  5. 5
    workup.DISTILLATIONThe solvent was distilled off
  6. 6
    ДругоеThe residue was purified by column chromatography (eluent: ethyl acetate)
  7. 7
    Другоеto obtain the powder which
  8. 8
    Промывкаwas washed with ether
  9. 9
    Другоеdried

Методика

To a solution of 1.00 g (4.15 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride and 2.77 ml (19.8 mmol) of triethylamine in 40 ml of methylene chloride was added 846 mg (4.96 mmol) of 4-anisoyl chloride under ice-cooling with stirring and the mixture was stirred for at room temperature for 30 minutes. The reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain the powder which was washed with ether and dried to obtain 990 mg of the desired compound (78.9%, colorless powder), mp: 121.0°-122.0° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05246948uspto-grants-1993_09