HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178465695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-(4-[2-Aminooxyethoxy)benzyl]thiazolidine-2,4-dione hydrochloride | HCID 21833965 | — |
| Reactant | HCID 178466812 | HCID 178466812 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178465695 | HCID 178465695 | 62.6% |
Reaction Steps
124 μl of pyridine were added at room temperature to a suspension of 100 mg of 3-acetyl-6-hydroxypyridine and 232 mg of 5-[4-(2-aminooxyethoxy)benzyl]thiazolidine-2,4-dione hydrochloride [prepared as described in step (e) above] in 10 ml of ethanol, and the resulting mixture was stirred and heated under reflux for 1 hour. At the end of this time, the reaction mixture was cooled to room temperature and the precipitate was collected by filtration to give 183 mg of the title compound as a crystalline powder, melting at 240-242° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05972959 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-f36c451dc0aa410b94ca7954bf573de3 |
| Source note | uspto-grants-1999_10 |