تفاعل #63363

ord-dab73a85ed0241b99c5dbb9c7a63b148

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITthe mixture is left
  2. 2
    workup.WAITto stand overnight at 0°-5°
  3. 3
    استخلاصExtraction
  4. 4
    غسيلthe organic phase is washed in succession with water, cold 2N hydrochloric acid, water, semi-saturated bicarbonate solution and water
  5. 5
    تجفيفAfter drying over magnesium sulphate
  6. 6
    ترشيحthe mixture is filtered
  7. 7
    تركيزconcentrated by evaporation
  8. 8
    أخرىthe residue is recrystallised from methanol

الإجراء التجريبي

A solution of 0.31 ml of methanesulphonic acid chloride in 3 ml of methylene chloride is added at room temperature to a solution of 1.03 g of 1-(4-aminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione and 24 mg of 4-dimethylaaminopyridine in 10 ml of pyridine. After stirring for 5 hours, 50 ml of water are added, and the mixture is left to stand overnight at 0°-5°. Extraction is carried out with methylene chloride, and the organic phase is washed in succession with water, cold 2N hydrochloric acid, water, semi-saturated bicarbonate solution and water. After drying over magnesium sulphate, the mixture is filtered and concentrated by evaporation, and the residue is recrystallised from methanol. The title compound is obtained in the form of white crystals having a melting point of 159°-160°. Rf (hexane/ethyl acetate 1:1)=0.15.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04764640uspto-grants-1988_08