반응 #4627

ord-fe8a390673e842ac9509d98d9cab3091

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타has been evaporated off
  2. 2
    기타The acidic, aqueous phase is separated off
  3. 3
    온도whilst cooling with ice
  4. 4
    추출extracted with ethyl acetate
  5. 5
    기타By separating off
  6. 6
    건조drying (MgSO4)
  7. 7
    농축concentrating the ethyl acetate
  8. 8
    추출extract by evaporation

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04727067uspto-grants-1988_02