Hydrochloric Acid → 3-ethyl-2-pyridin-3-yl-1H-indole

HRID 593509

Reaktionsgleichung

Reaktionsgleichung von HRID 593509
[C:1]1([NH:7]N)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15](=O)[CH2:16][CH2:17][CH3:18])[CH:10]=1.Cl>CCO>[CH2:17]([C:16]1[C:6]2[C:1](=[CH:2][CH:3]=[CH:4][CH:5]=2)[NH:7][C:15]=1[C:11]1[CH:10]=[N:9][CH:14]=[CH:13][CH:12]=1)[CH3:18]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 7516PhenylhydrazineHCID 4595021-(Pyridin-3-yl)butan-1-one

Produkt 1

HCID 582156283-ethyl-2-pyridin-3-yl-1H-indole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A flask is charged with phenylhydrazine (0.873 g, 6.46 mmol) and EtOH (14 mL). 1-Pyridin-3-yl-butan-1-one (0.914 g, 6.13 mmol) is added and the reaction is refluxed for 1 h. After cooling to room temperature, HCl (4M in 1,4-dioxane, 6.45 mL, 25.83 mmol) is added. The reaction mixture is refluxed for 4 h. After cooling to room temperature, the precipitate formed is filtered to afford 3-ethyl-2-pyridin-3-yl-1H-indole as a yellow solid. MS (ESI) m/z 223.0 (M+H)+.

Aufarbeitung

  1. temperaturethe reaction is refluxed for 1 h
  2. temperatureThe reaction mixture is refluxed for 4 h
  3. temperatureAfter cooling to room temperature
  4. customthe precipitate formed
  5. filtrationis filtered

Quellen und Nachweise

ORD-Eintrag
ord-7231d6a439804990987645806434c42f
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09242963B2

Verknüpfte Notizen

Wird geladen…