HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 58423146, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 58423110 | HCID 58423110 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58423146 | HCID 58423146 | 91.2% |
Reaction Steps
A 100 mL round bottom flask was charged with a magnetic stir bar, (S)-tert-butyl 1-(5-chloro-2-formylphenyl)pyrrolidin-3-ylcarbamate (Method 78) (1.100 g, 3.39 mmol), thiazolidine-2,4-dione (0.397 g, 3.39 mmol), and ethanol (11.29 ml). Piperidine (0.034 mL, 0.34 mmol) was added and the reaction was heated to reflux for 2 h. Once the reaction was judged to be complete by LCMS, it was allowed to cool to ambient temperature and conc. in vacuo to afford the title compound (1.310 g, 91%) which was used in the next step without further purification; m/z 425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901307B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-0593b3ec96e34b3e8f9605dbdb063578 |
| Source note | uspto-grants-2014_12 |