Ethyl 4-(pyridin-2-ylamino)piperidine-1-carboxylate → N-(Piperidin-4-yl)pyridin-2-amine
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH:7][CH:8]1[CH2:13][CH2:12][N:11](C(OCC)=O)[CH2:10][CH2:9]1>Br>[NH:11]1[CH2:12][CH2:13][CH:8]([NH:7][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)[CH2:9][CH2:10]1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
6 g of ethyl 4-(pyridin-2-ylamino)piperidine-1-carboxylate (23a) were refluxed in 30 ml of 47% HBr for 6 h. Evaporation of the mixture, trituration of the resulting crude product with ethyl acetate/CH3OH (9:1) and renewed drying afforded 7.1 g of white solid; ESI-MS [M+H+]=178.15.
Aufarbeitung
- customEvaporation of the mixture, trituration of the resulting crude product with ethyl acetate/CH3OH (9:1)
- customrenewed drying
Quellen und Nachweise
- ORD-Eintrag
- ord-a7ad09585266425da852695aa3693fbe
- Quelldatensatz
- uspto-grants-2006_10
- Patentnummer
- US07125883B1
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