Sodium Carbonate → 3-[4-[1-Hydroxyimino-2-(2-fluorophenyl)ethyl]piperidino]methyl-1H-pyrazin-2-one

HRID 606235Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 606235
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([CH:11]1[CH2:16][CH2:15][N:14]([CH2:17][C:18]2[C:19](=[O:24])[NH:20][CH:21]=[CH:22][N:23]=2)[CH2:13][CH2:12]1)=O.Cl.[NH2:26][OH:27].C(=O)([O-])[O-].[Na+].[Na+].[Cl-].[NH4+]>C(O)C.ClCCl.O>[OH:27][N:26]=[C:9]([CH:11]1[CH2:16][CH2:15][N:14]([CH2:17][C:18]2[C:19](=[O:24])[NH:20][CH:21]=[CH:22][N:23]=2)[CH2:13][CH2:12]1)[CH2:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[F:1]

Komponenten

8

Versuchsvorschrift

After suspending 150 mg of 3-[4-[2-(2-fluorophenyl)acetyl]piperidino]methyl-1H-pyrazin-2-one in 3 ml of ethanol, 47 mg of hydroxylamine hydrochloride and 193 mg of sodium carbonate were added while stirring and the mixture was heated to reflux for 1 hour. Water and saturated aqueous ammonium chloride solution were added to the reaction solution for adjustment to pH 7, and extraction was performed with dichloromethane. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. Diethyl ether was added and the insoluble portion was filtered out to obtain the title compound (109 mg, 70% yield).

Aufarbeitung

  1. additionwere added
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 1 hour
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. additionDiethyl ether was added
  8. filtrationthe insoluble portion was filtered out

Quellen und Nachweise

ORD-Eintrag
ord-ad6edbfcceb246069d75f0bd8728cc0d
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07915274B2

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