HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → 5-(2-Tritylaminothiazol-4-ylmethylene)thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(Tritylamino)thiazole-4-carbaldehyde | HCID 15053569 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(2-Tritylaminothiazol-4-ylmethylene)thiazolidine-2,4-dione | HCID 54351206 | — |
Reaction Steps
Following a procedure similar to that described in Example 17, the desired compound was prepared from 2 g of 2-tritylaminothiazole-4-carbaldehyde, 0.7 g of 2,4-thiazolidinedione, 1 g of piperidine and 20 ml of ethanol. The resulting product was a pale brown powder having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933355 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-26ad0fcea33d492ba071deefc4fee33c |
| Source note | uspto-grants-1990_06 |