Acetic Acid → N-(3-Methylphenyl)urea

HRID 963520노트

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HRID 963520 반응식
C1(C2C3C=CC=CC=3NC(=O)C([NH:20][C:21]([NH:23][C:24]3[CH:29]=[CH:28][CH:27]=[C:26]([CH3:30])[CH:25]=3)=[O:22])N=2)CCCCCC1.BrCC(N1CC2CCC(CC2)C1)=O.[H-].[Na+].C(O)(=O)C>CN(C)C=O>[CH3:30][C:26]1[CH:25]=[C:24]([NH:23][C:21](=[O:22])[NH2:20])[CH:29]=[CH:28][CH:27]=1

참가 물질

6

실험 절차

To a solution of N-[(3RS)-5-cycloheptyl-2,3-dihydro-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-(3-methylphenyl)urea (0.102 g) and N-bromomethylcarbonyl-3-azabicyclo[3.2.2]nonane (0.079 g) in dry N,N-dimethylformamide (10 ml) was added sodium hydride (0.011 g of a 63.8% dispersion in mineral oil) at 5°-10° C. The mixture was stirred at the same temperature for 30 minutes and then at ambient temperature overnight. The resultant mixture was treated with 0.1 g of acetic acid at room temperature for 30 minutes and then concentrated in vacuo. The residue was disolved with ethyl acetate (100 ml) and washed with saturated sodium hydrogen carbonate aqueous solution (20 ml) and a brine (20 ml). The organic layer was dried over magnesium sulfate. Filtration and evaporation gave a crude product. The crude product was purified by column chromatography on silica gel with chloroform and a mixture of chloroform and ethyl acetate (5:1) as eluents to afford N-[(3RS)-1-[(3-azabicyclol3.2.2]non-3-yl)carbonylmethyl]-5-cycloheptyl-2,3-dihydro-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-(3-methylphenyl)urea (0.090 g).

후처리

  1. customat ambient temperature
  2. customovernight
  3. concentrationconcentrated in vacuo
  4. washwashed with saturated sodium hydrogen carbonate aqueous solution (20 ml)
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. filtrationFiltration and evaporation
  7. customgave a crude product
  8. customThe crude product was purified by column chromatography on silica gel with chloroform
  9. additiona mixture of chloroform and ethyl acetate (5:1) as eluents

출처 및 근거

ORD 기록
ord-4f60d0453eef4bdab80956bb0ce2120a
출처 데이터셋
uspto-grants-1998_06
특허 번호
US05763437

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