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Ethyl isothiocyanatoformate → 1-Ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea

HRID 1415638
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HRID 1415638 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:14])[CH2:10][N:11]([CH3:13])[CH3:12].[CH2:15]([O:17][C:18]([N:20]=[C:21]=[S:22])=[O:19])[CH3:16]>C(#N)C>[CH2:15]([O:17][C:18]([NH:20][C:21]([NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9](=[O:14])[CH2:10][N:11]([CH3:12])[CH3:13])=[S:22])=[O:19])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 85320Ethyl isothiocyanatoformateHCID 16784338N-(2-aminophenyl)-2-(dimethylamino)acetamide

생성물 1

HCID 214829821-Ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea수율 62.9%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A suspension of N-(2-aminophenyl)-2-dimethylaminoacetamide (8.9 g) (prepared as described in Example 6) in acetonitrile (50 ml) was treated with ethoxycarbonyl isothiocyanate (6.4 g), dropwise with stirring, maintaining the temperature at 15°-20° C. by external cooling. When the addition was complete, the solid had dissolved but after being left to stand for a further 5 minutes, another solid precipitated. This was filtered off and washed with ice-cold acetonitrile to give 1-ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea (9.4 g), m.p. 159°-160° C. (with decomposition).

후처리

  1. temperaturemaintaining the temperature at 15°-20° C. by external cooling
  2. additionWhen the addition
  3. dissolutionthe solid had dissolved
  4. waitafter being left
  5. customanother solid precipitated
  6. filtrationThis was filtered off
  7. washwashed with ice-cold acetonitrile

출처 및 근거

ORD 기록
ord-dad36edf293c4c5eaabc06dca4f775b0
출처 데이터셋
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04005217

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