Ethanol → HCID 18317742, Verbindung

HRID 1700686Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1700686
ClC1C=CC=CC=1C1C[C:12](=O)[C:11](=[C:15](O)[CH3:16])C(=O)C1.[ClH:19].N(N=[C:25]1[CH2:33][CH:32]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[CH2:31][C:30]2[NH:29][CH:28]=[C:27]([CH3:40])[C:26]1=2)C(N)=N.[CH2:41]([N:43](CC)CC)[CH3:42].C([OH:50])C>>[CH2:28]([N:29]1[C:30]2[CH2:31][CH:32]([C:34]3[CH:35]=[CH:36][CH:37]=[CH:38][C:39]=3[Cl:19])[CH2:33][C:25](=[O:50])[C:26]=2[C:41]([CH3:42])=[N:43]1)[C:27]1[CH:40]=[CH:12][CH:11]=[CH:15][CH:16]=1

Komponenten

5

Versuchsvorschrift

To a solution of 5-(2-chlorophenyl)-2-(1-hydroxyethylidene)cyclohexane-1,3-dione (0.5 g) and benzylhydrazine 2 hydrochloride (0.39 g) in ethanol (30 ml) was added triethylamine (0.42 g), and the mixture was refluxed for 2.5 hours. Under reduced pressure, the solvent was evaporated, and the residue was dissolved in ethyl acetate. The organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure, and the residue was purified with silica gel column chromatography (ethyl acetate-hexane). The resulting crystals were recrystallized from ethyl acetate-hexane to give 1-benzyl-6-(2-chlorophenyl)-3-methyl-4,5,6,7-tetrahydroindazol-4-one (0.37 g) as colorless crystals.

Aufarbeitung

  1. temperaturethe mixture was refluxed for 2.5 hours
  2. customUnder reduced pressure, the solvent was evaporated
  3. dissolutionthe residue was dissolved in ethyl acetate
  4. washThe organic layer was washed with water and saturated brine
  5. dry with materialdried with magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customthe residue was purified with silica gel column chromatography (ethyl acetate-hexane)
  8. customThe resulting crystals were recrystallized from ethyl acetate-hexane

Quellen und Nachweise

ORD-Eintrag
ord-60d4f62dd6514c8eb263f1ed4c0a5848
Quelldatensatz
uspto-grants-2002_02
Patentnummer
US06350749B1

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