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4-Fluorophenylhydrazine hydrochloride → 1-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine

HRID 83493
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HRID 83493 반응식
[F:1][C:2]([F:15])([F:14])[O:3][C:4]1[CH:5]=[C:6](/[CH:10]=[CH:11]/[C:12]#[N:13])[CH:7]=[CH:8][CH:9]=1.FC(F)(F)OC1C=C(/C=C\C#N)C=CC=1.Cl.[F:32][C:33]1[CH:38]=[CH:37][C:36]([NH:39][NH2:40])=[CH:35][CH:34]=1.[O-]CC.[Na+]>C(O)C>[F:32][C:33]1[CH:38]=[CH:37][C:36]([N:39]2[CH:10]([C:6]3[CH:7]=[CH:8][CH:9]=[C:4]([O:3][C:2]([F:14])([F:15])[F:1])[CH:5]=3)[CH2:11][C:12]([NH2:13])=[N:40]2)=[CH:35][CH:34]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 699814-Fluorophenylhydrazine hydrochlorideHCID 2723922Sodium ethoxideHCID 86680352(E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrileHCID 86680353(Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile

생성물 1

HCID 712877431-(4-Fluorophenyl)-5-(3-(trifluoromethoxy)phenyl)-4,5-dihydro-1H-pyrazol-3-ylamine

시약·촉매·용매 1

HCID 702
Ethanol
용매

실험 절차

To a solution of a mixture of (E)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile and (Z)-3-(3-(trifluoromethoxy)phenyl)acrylonitrile (1.28 g) in ethanol (13 ml) were sequentially added 4-fluorophenylhydrazine hydrochloride (979 mg) and sodium ethoxide (20 wt % in ethanol, 5.0 ml), and the mixture was stirred overnight at reflux. This reaction solution was concentrated under reduced pressure, and then water was added thereto, and the mixture was extracted with ethyl acetate. This organic layer was sequentially washed with water and a saturated aqueous solution of sodium chloride, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1 to 1/1) to give the titled compound (1.29 g).

후처리

  1. temperatureat reflux
  2. concentrationThis reaction solution was concentrated under reduced pressure
  3. additionwater was added
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThis organic layer was sequentially washed with water
  6. concentrationa saturated aqueous solution of sodium chloride, and then concentrated under reduced pressure
  7. customThe resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1 to 1/1)

출처 및 근거

ORD 기록
ord-afc7bcc94e5c4b498feaeb05f2571b71
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846746B2

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