Potassium Hydroxide → HCID 22611373, Verbindung

HRID 1737766Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1737766
[OH-].[K+].[O:3]1[CH:7]=[CH:6][CH:5]=[C:4]1[C:8]([NH:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[NH:16][CH:15]=[CH:14]2)=[O:9].[CH2:20]([N:22]1[CH2:27][CH2:26][C:25](=O)[CH2:24][CH2:23]1)C>CO>[O:3]1[CH:7]=[CH:6][CH:5]=[C:4]1[C:8]([NH:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[NH:16][CH:15]=[C:14]2[C:25]1[CH2:26][CH2:27][N:22]([CH3:20])[CH2:23][CH:24]=1)=[O:9]

Komponenten

5

Edukt 3

HCID 14797Potassium HydroxideHCID 771591-Ethylpiperidin-4-oneHCID 22611244HCID 22611244, Verbindung

Produkt 1

HCID 22611373HCID 22611373, VerbindungAusbeute 48,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 0.868 gm (15.5 mMol) potassium hydroxide in 8 mL methanol were added 1.0 gm (4.42 mMol) 5-(2-furoyl)amino-1H-indole and 0.774 mL 1-ethyl-4-piperidone and the solution was stirred at reflux for 18 hours. The reaction mixture was cooled to ambient and then diluted with ice/water. The resultant precipitate was collected and dried under vacuum. This solid was purified by radial chromatography (2 mm silica), eluting with a gradient of dichloromethane containing 5-7.5% methanol and 0.5-1.0% ammonium hydroxide. The product was then crystallized from ethyl acetate to give 0.715 gm (48.3%) of the title compound as a bright yellow powder.

Aufarbeitung

  1. temperatureat reflux for 18 hours
  2. temperatureThe reaction mixture was cooled to ambient and
  3. customThe resultant precipitate was collected
  4. customdried under vacuum
  5. customThis solid was purified by radial chromatography (2 mm silica)
  6. washeluting with a gradient of dichloromethane containing 5-7.5% methanol and 0.5-1.0% ammonium hydroxide
  7. customThe product was then crystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-070b13d9a4e44adeb401badc4ea44c9b
Quelldatensatz
uspto-grants-1999_10
Patentnummer
US05962474

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