Réaction #63363

Équation de réaction

methanesulphonic acid chloride

1-(4-aminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione

water

→

title compound

1-(4-methanesulphonylaminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione

Solvants

methylene chloride

pyridine

Conditions de réaction

Traitement

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

Mode opératoire

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.

Source