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Cyclopropanecarbonyl chloride → 1-Cyclopropancarboamide 2-(3-methoxycarbonyl-2-thioureido)-benzene

HRID 1414426
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반응식

HRID 1414426 반응식
[CH:1]1([C:4](Cl)=[O:5])[CH2:3][CH2:2]1.[NH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15]([NH:17][C:18]([O:20][CH3:21])=[O:19])=[S:16]>>[CH:1]1([C:4]([NH2:7])=[O:5])[CH2:3][CH2:2]1.[CH3:21][O:20][C:18]([NH:17][C:15](=[S:16])[NH:14][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:8]=1)=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 77637Cyclopropanecarbonyl chlorideHCID 3032830Thiophamine

생성물 1

HCID 867343571-Cyclopropancarboamide 2-(3-methoxycarbonyl-2-thioureido)-benzene

실험 절차

3.5g (0.033 mole) of cyclopropylcarbonylchloride were added slowly to 5.6g (0.025 mole) of 1-(2-aminophenyl)-3-methoxycarbonyl-2-thiourea in 30ml of tonuene at room temperature under agitation and the mixture was kept on reflux condition for an hour. The reaction mixture was cooled to room temperature and filtered with suction. The recovered colorless crystals were washed with water and dried. Then, by recrystallization of the crystals from the mixture of methanol and acetone, 4.2g of the crystals having the decomposition point of 191° - 192° C. were obtained.

후처리

  1. temperatureon reflux condition for an hour
  2. filtrationfiltered with suction
  3. washThe recovered colorless crystals were washed with water
  • customdried
  • customThen, by recrystallization of the crystals
  • additionfrom the mixture of methanol and acetone, 4.2g of the crystals
  • customwere obtained
  • 출처 및 근거

    ORD 기록
    ord-c2aa1ff2a0a944efb1c6d5a1d0e8fe14
    출처 데이터셋
    uspto-grants-1977_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04001297

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