HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanal → 5-Butylidene-3-(imidazo[1,2-a]pyridin-5-yl)methylthiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-(Imidazo[1,2-a]pyridin-5-yl)methylthiazolidine-2,4-dione | HCID 18936860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Butylidene-3-(imidazo[1,2-a]pyridin-5-yl)methylthiazolidine-2,4-dione | HCID 57284540 | — |
Reaction Steps
To a solution of 223 mg (0.9 mmol) of 3-(imidazo[1,2-a]pyridin-5-yl)methylthiazolidine-2,4-dione and 0.09 ml (1.0 mmol) of n-butyraldehyde in 5 ml of ethanol, 0.001 ml (0.1 mmol) of piperidine was added, followed by refluxing for 2 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in chloroform, washed with water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, hexane/ethyl acetate=1/4) to yield 222 mg (82.2%, light yellow oily substance) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840732 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-7f2d08878ffa4385aea68ddacfdaeb82 |
| Source note | uspto-grants-1998_11 |