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Acetonitrile → Ranisen

HRID 65765
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HRID 65765 반응식
[CH3:1][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][S:11][CH2:12][CH2:13][NH2:14])=[CH:7][CH:6]=1)[CH3:3].CS[C:17](SC)=[CH:18][N+:19]([O-:21])=[O:20].[C:24](#[N:26])C>>[CH3:3][N:2]([CH2:4][C:5]1[O:9][C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:17]([NH:26][CH3:24])=[CH:18][N+:19]([O-:21])=[O:20])=[CH:7][CH:6]=1)[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6342AcetonitrileHCID 836231,1-Bis(methylthio)-2-nitroethyleneHCID 1622035-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine

생성물 1

HCID 5039Ranisen

실험 절차

2-[[[5-(Dimethylamino)methyl-2-furanyl]methyl]thio]ethanamine (4.25 g) and 1,1-bis(methylthio)-2-nitroethene (3.3 g) were refluxed in acetonitrile (50 ml) for 14 hr. Solvent was removed and the residue dissolved in 36% methanolic methylamine (50 ml) and the solution refluxed for 8 hr. Solvents were removed and the residue in methanol treated with charcoal. Filtration and evaporation of the solvent gave the title compound as Example 15 (5.0 g).

후처리

  1. customSolvent was removed
  2. dissolution
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
the residue dissolved in 36% methanolic methylamine (50 ml)
  • temperaturethe solution refluxed for 8 hr
  • customSolvents were removed
  • additionthe residue in methanol treated with charcoal
  • filtrationFiltration and evaporation of the solvent
  • 출처 및 근거

    ORD 기록
    ord-590ae28d589b41ae960292662b4c4b89
    출처 데이터셋
    uspto-grants-1978_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04128658

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