Hydrogen chloride-ethyl acetate → 5-Propylidene-3-[4-(imidazo[1,2-a]pyridin-8-yloxy)butyl]-thiazolidine-2,4-dione hydrochloride
Reaktionsgleichung
[CH:1](=[C:4]1[S:8][C:7](=[O:9])[N:6]([CH2:10][CH2:11][CH2:12][CH2:13][O:14][C:15]2[C:16]3[N:17]([CH:21]=[CH:22][N:23]=3)[CH:18]=[CH:19][CH:20]=2)[C:5]1=[O:24])[CH2:2][CH3:3].[ClH:25].C(OCC)(=O)C>CO>[ClH:25].[CH:1](=[C:4]1[S:8][C:7](=[O:9])[N:6]([CH2:10][CH2:11][CH2:12][CH2:13][O:14][C:15]2[C:16]3[N:17]([CH:21]=[CH:22][N:23]=3)[CH:18]=[CH:19][CH:20]=2)[C:5]1=[O:24])[CH2:2][CH3:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a methanol solution of 0.691 g (2.0 mmol) of 5-propylidene-3-[4-(imidazo[1,2-a]pyridin-8-yloxy)butyl]thiazolidine-2,4-dione, 0.5 ml of 4N hydrochloric acid-ethyl acetate was added, followed by stirring. After the solvent was distilled off, the residue was washed with ether to yield 0.79 g (quant., yellow oily substance) of the desired product.
Aufarbeitung
- distillationAfter the solvent was distilled off
- washthe residue was washed with ether
Quellen und Nachweise
- ORD-Eintrag
- ord-a833122e35e340dd890cd09ac4760f80
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05840732
Notizen zur Reaktion
Wird geladen…