Reaktionsgleichung
[CH2:1]([N:3]([CH2:6][C:7]1[O:28][C:10]2[CH2:11][N:12]([C:15](=[O:27])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH2:13][CH2:14][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2].[ClH:29]>CO>[ClH:29].[CH2:1]([N:3]([CH2:6][C:7]1[O:28][C:10]2[CH2:11][N:12]([C:15](=[O:27])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH2:13][CH2:14][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1-(2-Diethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one 0.178 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol was added in excess, followed by stirring. This mixture was concentrated to yield the desired product.
Aufarbeitung
- concentrationThis mixture was concentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-404ee9f641344e9bb502b6be92848703
- Quelldatensatz
- uspto-grants-1999_12
- Patentnummer
- US05998433
Verknüpfte Notizen
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