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Phenylhydrazine → 4-(5-amino-1-phenyl-1H-pyrazole-3-yl)-benzoic acid methyl ester

HRID 1860521
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인쇄 미리보기

반응식

HRID 1860521 반응식
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH2:11][C:12]#[N:13])=[CH:6][CH:5]=1.[C:16]1([NH:22][NH2:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(O)C>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[C:12]([NH2:13])[N:22]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[N:23]=2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7516PhenylhydrazineHCID 736021Methyl 4-(cyanoacetyl)benzoate

생성물 1

HCID 698301914-(5-amino-1-phenyl-1H-pyrazole-3-yl)-benzoic acid methyl ester

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of methyl-4-(cyanoacetyl)benzoate (5.0 g, 24.6 mmol) and phenylhydrazine (2.42 ml, 24.6 mmol) in ethanol (100 ml) was heated to reflux for 20 hours. The mixture was cooled and the product was collected by filtration. The product was purified by trituration in hot acetonitrile, cooled and collected by filtration to give the product 4-(5-amino-1-phenyl-1H-pyrazole-3-yl)-benzoic acid methyl ester as a colorless solid.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 20 hours
  3. temperatureThe mixture was cooled
  4. filtrationthe product was collected by filtration
  5. customThe product was purified by trituration in hot acetonitrile
  6. temperaturecooled
  7. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-891129d41585444f8cf20e5012374e98
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06531478B2

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