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Acetic Anhydride → N-[3-(1,6-Dihydro-6-oxo-3-pyridazinyl)phenyl]acetamide

HRID 35625
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HRID 35625 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:9]=[CH:10][C:11](=[O:14])[NH:12][N:13]=2)[CH:5]=[CH:6][CH:7]=1.[C:15](OC(=O)C)(=[O:17])[CH3:16]>>[O:14]=[C:11]1[NH:12][N:13]=[C:8]([C:4]2[CH:3]=[C:2]([NH:1][C:15](=[O:17])[CH3:16])[CH:7]=[CH:6][CH:5]=2)[CH:9]=[CH:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 113444556-(3-Aminophenyl)-2,3-dihydropyridazin-3-one

생성물 1

HCID 15595699N-[3-(1,6-Dihydro-6-oxo-3-pyridazinyl)phenyl]acetamide

실험 절차

A mixture of 37 g of 6-(3-aminophenyl)-3(2H)-pyridazinone and 500 ml of acetic anhydride was heated at 85°-90° C. for 8 hours. The solvent was removed in vacuo and the residue dissolved in 500 ml of methanol. To this solution was added portionwise 40 g of potassium hydroxide. The solution was refluxed for 3 hours and the solvent removed in vacuo. The residue was dissolved in water and the solution neutralized with hydrochloric acid. The resulting solid was collected and recrystallized from dichloromethane-methanol, giving 10.8 g of the desired compound as crystals, mp 250°-252° C. (dec.).

후처리

  1. temperaturewas heated at 85°-90° C. for 8 hours
  2. customThe solvent was removed in vacuo
dissolution
the residue dissolved in 500 ml of methanol
  • additionTo this solution was added portionwise 40 g of potassium hydroxide
  • temperatureThe solution was refluxed for 3 hours
  • customthe solvent removed in vacuo
  • dissolutionThe residue was dissolved in water
  • customThe resulting solid was collected
  • customrecrystallized from dichloromethane-methanol
  • 출처 및 근거

    ORD 기록
    ord-4693b9de569d4a6cbf62c8ff01cdb088
    출처 데이터셋
    uspto-grants-1988_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04767765

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