Hydrochloric Acid → 5-(Piperidin-1-yl)methylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione dihydrochloride
Reaktionsgleichung
[N:1]1([CH:7]=[C:8]2[S:12][C:11](=[O:13])[N:10]([CH2:14][CH2:15][CH2:16][CH2:17][S:18][C:19]3[N:24]4[CH:25]=[CH:26][N:27]=[C:23]4[CH:22]=[CH:21][CH:20]=3)[C:9]2=[O:28])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[ClH:29]>CO>[ClH:29].[ClH:29].[N:1]1([CH:7]=[C:8]2[S:12][C:11](=[O:13])[N:10]([CH2:14][CH2:15][CH2:16][CH2:17][S:18][C:19]3[N:24]4[CH:25]=[CH:26][N:27]=[C:23]4[CH:22]=[CH:21][CH:20]=3)[C:9]2=[O:28])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 220 mg (0.526 mmol) of 5-(piperidin-1-yl)methylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]-thiazolidine-2,4-dione in 10 ml of methanol, concentrated hydrochloric acid was added. After the solvent was distilled off, the residue was washed with diethyl ether to yield 218 mg (56.2%, white powder) of the desired product.
Aufarbeitung
- distillationAfter the solvent was distilled off
- washthe residue was washed with diethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-f2064200e2844891921a6d8988fb5693
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05840732
Notizen zur Reaktion
Wird geladen…