Hydrochloric Acid → 1-(Pyridin-4-yl)piperidine-3-carboxylic acid hydrochloride
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][C:4]([N:7]2[CH2:12][CH2:11][CH2:10][CH:9]([C:13]([O:15]CC)=[O:14])[CH2:8]2)=[CH:3][CH:2]=1.[ClH:18]>O1CCOCC1>[ClH:18].[N:1]1[CH:2]=[CH:3][C:4]([N:7]2[CH2:12][CH2:11][CH2:10][CH:9]([C:13]([OH:15])=[O:14])[CH2:8]2)=[CH:5][CH:6]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 1.8 g of ethyl 1-(4-pyridyl)-piperidine-3-carboxylate, 50 ml of dioxane and 20 ml of 1 M hydrochloric acid was heated under reflux for 5 hours. The solvent was evaporated, and the residue was washed with ethyl acetate to obtain the title compound.
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux for 5 hours
- customThe solvent was evaporated
- washthe residue was washed with ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-8e3b448397e646fe82b0b737be53b5bf
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06710056B2
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