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Ethylenediamine → HCID 21463158, 화합물

HRID 1940979
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HRID 1940979 반응식
O=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:4]([C:18]([OH:20])=O)[O:3]1.[CH2:21]([NH2:24])[CH2:22][NH2:23]>>[O:20]=[C:18]1[C:4]2[N:24]([C:2](=[O:3])[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=3[C:5]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:21][CH2:22][NH:23]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 3301EthylenediamineHCID 42017421-oxo-4-phenyl-1H-isochromene-3-carboxylic acid

생성물 1

HCID 21463158HCID 21463158, 화합물

실험 절차

A mixture of 1-oxo-4-phenyl-1H-2-benzopyran-3-carboxylic acid (500 mg) and ethylenediamine (15 ml) was stirred at room temperature overnight. After evaporation of the solvent, concentrated hydrochloric acid (10 ml) and acetic acid (10 ml) were added to the residue. The mixture was heated under reflux for 48 hours. To the mixture was added water, and extracted with ethyl acetate. The extract was washed successively with water, aqueous sodium hydrogen carbonate and water, dried, and evaporated to yield the title compound as colorless crystals (115 mg).

후처리

  1. customAfter evaporation of the solvent, concentrated hydrochloric acid (10 ml) and acetic acid (10 ml)
  2. additionwere added to the residue
  3. temperatureThe mixture was heated
  4. temperature
under reflux for 48 hours
  • additionTo the mixture was added water
  • extractionextracted with ethyl acetate
  • washThe extract was washed successively with water, aqueous sodium hydrogen carbonate and water
  • customdried
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-ea8907fe1ee34b42b5b4d859cd674457
    출처 데이터셋
    uspto-grants-1997_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05700810

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