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1-Acetylnaphthalene → 5-Methyl-2-[3-(1-naphthyl)-3-oxo-1-propenyl]-4-piperidinopyridine

HRID 1904655
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1904655
[OH-].[Na+].[C:3]([C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8][CH:7]=1)(=[O:5])[CH3:4].[CH3:16][C:17]1[C:18]([N:25]2[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]2)=[CH:19][C:20]([CH:23]=O)=[N:21][CH:22]=1>CO>[CH3:16][C:17]1[C:18]([N:25]2[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]2)=[CH:19][C:20]([CH:23]=[CH:4][C:3]([C:6]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:9]=[CH:8][CH:7]=2)=[O:5])=[N:21][CH:22]=1
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Komponenten

5

Edukt 3

HCID 136631-AcetylnaphthaleneHCID 14798Sodium HydroxideHCID 200375995-Methyl-4-piperidino-2-pyridinecarbaldehyde

Produkt 1

HCID 537670295-Methyl-2-[3-(1-naphthyl)-3-oxo-1-propenyl]-4-piperidinopyridine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A 10% aqueous solution of sodium hydroxide (1.6 ml) and then 174 mg of 1-acetylnaphthalene at about 4° C. were added to a solution of 204 mg (1.0 mmole) of 5-methyl-4-piperidino-2-pyridinecarbaldehyde in 3 ml of methanol, and the mixture was allowd to stand overnight at the above temperature. The reaction mixture was concentrated under reduced pressure. The residue was mixed with water, and then extracted with dichloromethane. The dichloromethane layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluted with dichloromethane) to give 5-methyl-2-[3-(1-naphthyl)-3-oxo-1-propenyl]-4-piperidinopyridine. The product was treated with an ethanol solution of hydrogen chloride to form its hydrochloride. Recrystallization from methanol/ether gave 350 mg (yield 75%) of the captioned compound as crystals.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionThe residue was mixed with water
  3. extractionextracted with dichloromethane
  4. dry with materialThe dichloromethane layer was dried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (eluted with dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-93448bd2bccd454486a47019453ee87f
Quelldatensatz
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04839353

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