Réaction #4627

Équation de réaction

6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one

4-(2,3-epoxypropoxy)-N-methylbenzamide

→

1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol

Solvants

isopropanol

Conditions de réaction

Traitement

1. 1
   Autrehas been evaporated off
2. 2
   AutreThe acidic, aqueous phase is separated off
3. 3
   Températurewhilst cooling with ice
4. 4
   Extractionextracted with ethyl acetate
5. 5
   AutreBy separating off
6. 6
   Séchagedrying (MgSO4)
7. 7
   Concentrationconcentrating the ethyl acetate
8. 8
   Extractionextract by evaporation

Mode opératoire

A solution of 13.6 g of 6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one and 10.4 g of 4-(2,3-epoxypropoxy)-N-methylbenzamide in 80 ml of isopropanol is refluxed for 30 hours. The residue remaining after the solvent has been evaporated off is divided between ether and 2N hydrochloric acid. The acidic, aqueous phase is separated off, and, whilst cooling with ice, rendered alkaline with approximately 10% aqueous ammonia solution and extracted with ethyl acetate. By separating off, drying (MgSO4) and concentrating the ethyl acetate extract by evaporation, the crude 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-methylcarbamoylphenoxy)propan-2-ol is obtained as an oil which may be used without further purification for catalytic debenzylation.

Source