تفاعل #4627

ord-fe8a390673e842ac9509d98d9cab3091

معادلة التفاعل

CC(COc1ccc2c(c1)C(=O)NC(C)(C)O2)NCc1ccccc1
6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one
CNC(=O)c1ccc(OCC2CO2)cc1
4-(2,3-epoxypropoxy)-N-methylbenzamide
CNC(=O)c1ccc(OCC(O)CN(Cc2ccccc2)C(C)COc2ccc3c(c2)C(=O)NC(C)(C)O3)cc1
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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىhas been evaporated off
  2. 2
    أخرىThe acidic, aqueous phase is separated off
  3. 3
    درجة الحرارةwhilst cooling with ice
  4. 4
    استخلاصextracted with ethyl acetate
  5. 5
    أخرىBy separating off
  6. 6
    تجفيفdrying (MgSO4)
  7. 7
    تركيزconcentrating the ethyl acetate
  8. 8
    استخلاصextract by evaporation

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727067uspto-grants-1988_02