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2-(Ethoxymethylene)propanedinitrile → 5-amino-1-(2,3,4-trichlorophenyl)-1H-pyrazole-4-carbonitrile

HRID 2413082
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HRID 2413082 반응식
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([Cl:9])[CH:5]=[CH:4][C:3]=1[NH:10][NH2:11].C(O[CH:15]=[C:16]([C:19]#[N:20])[C:17]#[N:18])C>C(O)C>[NH2:20][C:19]1[N:10]([C:3]2[CH:4]=[CH:5][C:6]([Cl:9])=[C:7]([Cl:8])[C:2]=2[Cl:1])[N:11]=[CH:15][C:16]=1[C:17]#[N:18]
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참가 물질

4

반응물 2

HCID 671522-(Ethoxymethylene)propanedinitrileHCID 129529942,3,4-Trichlorophenylhydrazine

생성물 1

HCID 30189015-amino-1-(2,3,4-trichlorophenyl)-1H-pyrazole-4-carbonitrile수율 43.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2,3,4-Trichlorophenylhydrazine (21.15 g) was added in portions to a refluxing solution of ethoxymethylenemalononitrile (12.2 g) in ethanol (100 ml). The solution obtained was then heated at reflux for one hour, cooled and evaporated to dryness. The residue thus obtained was triturated with diethyl ether (100 ml) to give 5-amino-4-cyano-1-(2,3,4-trichlorophenyl)pyrazole (12.6 g), m.p. 158°-160° C., in the form of light brown crystals.

후처리

  1. customThe solution obtained
  2. temperaturewas then heated
  3. temperatureat reflux for one hour
  4. temperaturecooled
  5. customevaporated to dryness
  6. customThe residue thus obtained
  7. customwas triturated with diethyl ether (100 ml)

출처 및 근거

ORD 기록
ord-a61e8b70fc864e9abc69720a9cad9f98
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04496390

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