HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357093Erstellt: 24. Oktober 2026
Benzenepropanal → 5-(3-Phenylpropylidene)-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione
https://huagongshe.com/de/reaction/357093
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzenepropanal | HCID 7707 | — |
| Edukt | Pyrrolidine | HCID 31268 | — |
| Edukt | 3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione | HCID 18936736 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-(3-Phenylpropylidene)-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione | HCID 57260764 | — |
Reaktionsschritte
1.53 g (5 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione and 20 ml of ethanol were placed in a reaction flask, followed by stirring at 60° C. for 20 minutes, to dissolve the starting materials. After this mixture was kept standing to 50° C., an ethanol solution of 0.05 ml (0.5 mmol) of pyrrolidine was added. Next, an ethanol solution of 0.66 ml (5 mmol) of 3-phenylpropionaldehyde was added, followed by refluxing for 19 hours. Six hours later, 0.66 ml (5 mmol) of 3-phenylpropionaldehyde and 0.05 ml (0.5 mmol) of pyrrolidine were added. After the reaction mixture was cooled, the solvent was distilled off, followed by extraction with dichloromethane and water. After the organic layer was dried with sodium sulfate, the solvent was distilled off. The residue was eluted by column chromatography (eluent, hexane/ethyl acetate=1/1) to yield 26 mg (1.2%, yellow oily substance) of the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05840732 |
|---|
| Quelldatensatz | uspto-grants-1998_11 |
|---|
| ORD ID | ord-dcae2e9c56c2411b9f4c9ab2d1acd2d0 |
|---|
| Quellennotiz | uspto-grants-1998_11 |
|---|