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

HRID 1414426
ノート
印刷プレビュー

反応式

HRID 1414426 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 77637Cyclopropanecarbonyl chlorideHCID 3032830Thiophamine

生成物 1

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

実験手順

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.

後処理

  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
  • 出典と根拠

    ORDレコード
    ord-c2aa1ff2a0a944efb1c6d5a1d0e8fe14
    出典データセット
    uspto-grants-1977_01
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04001297

    反応ノート

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