HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 74348953, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | HCID 86654536 | HCID 86654536 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 74348953 | HCID 74348953 | — |
Reaction Steps
To 4-benzooxazol-2-yl-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine-7-carbaldehyde [compound of Step VI] (0.176 g, 0.6 mmol) taken in toluene (25 mL) were added 2,4-thiazolidine dione (0.105 g, 0.9 mmol) and catalytic amount of piperidinium acetate (0.025 g). The resulting mixture was refluxed under Dean Stark conditions for 1.5 hours and then cooled in an ice-bath. The precipitate was filtered and washed with toluene and petroleum ether to give 5-(4-benzooxazol-2-yl-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-7-ylmethylene)-thiazolidine-2,4-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263587B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-878ac6f22dea4cf88896500d4a61f3b8 |
| Source note | uspto-grants-2012_09 |