Hydrochloric Acid → 6-[4-(1-Phenylethenyl)benzoyl]-2-(1-pyrrolidinylmethyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridine hydrochloride
Reaktionsgleichung
[C:1]1([C:7]([C:9]2[CH:31]=[CH:30][C:12]([C:13]([N:15]3[CH2:20][CH2:19][C:18]4[CH:21]=[C:22]([CH2:24][N:25]5[CH2:29][CH2:28][CH2:27][CH2:26]5)[O:23][C:17]=4[CH2:16]3)=[O:14])=[CH:11][CH:10]=2)=[CH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:32]>CO>[ClH:32].[C:1]1([C:7]([C:9]2[CH:10]=[CH:11][C:12]([C:13]([N:15]3[CH2:20][CH2:19][C:18]4[CH:21]=[C:22]([CH2:24][N:25]5[CH2:29][CH2:28][CH2:27][CH2:26]5)[O:23][C:17]=4[CH2:16]3)=[O:14])=[CH:30][CH:31]=2)=[CH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
6-[4-(1-Phenylethenyl)benzoyl]-2-(1-pyrrolidinylmethyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridine 0.688 g was dissolved in 2 ml of methanol and hydrogen chloride in methanol was added in excess, followed by stirring. This mixture was concentrated to yield the desired product.