Hydrochloric Acid → 5-(Dimethylamino)methylene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione dihydrochloride
Reaktionsgleichung
[CH3:1][N:2]([CH:4]=[C:5]1[S:9][C:8](=[O:10])[N:7]([CH2:11][CH2:12][CH2:13][CH2:14][S:15][C:16]2[N:21]3[CH:22]=[CH:23][N:24]=[C:20]3[CH:19]=[CH:18][CH:17]=2)[C:6]1=[O:25])[CH3:3].[ClH:26]>CO>[ClH:26].[ClH:26].[CH3:1][N:2]([CH:4]=[C:5]1[S:9][C:8](=[O:10])[N:7]([CH2:11][CH2:12][CH2:13][CH2:14][S:15][C:16]2[N:21]3[CH:22]=[CH:23][N:24]=[C:20]3[CH:19]=[CH:18][CH:17]=2)[C:6]1=[O:25])[CH3:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 310 mg (0.823 mmol) of 5-(dimethylamino)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 311 mg (84.1%, 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-6f729da9927e490292e5feca1d7854ae
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05840732
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