HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 13339906, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Thiazolidine | HCID 10444 | — |
| Reactant | 1-Ethyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 800521 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13339906 | HCID 13339906 | 10.1% |
Reaction Steps
A solution of 1.01 g (4.0 mmol) of 1-ethyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 0.79 ml (10 mmol) of thiazolidine, 20 ml of acetonitrile and 20 ml of N,N-dimethylformamide was heated at reflux for 16 hours. The reaction was cooled to room temperature and the solid which formed was removed by filtration. After triturating with hot methanol, the residue was recrystallized from N,N-dimethylformamide to give 0.13 g of 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(3-thiazolidinyl)-3-quinolinecarboxylic acid; mp 270°-273° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04473568 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-a73e241a13ba46348fb733c2f79b54f7 |
| Source note | uspto-grants-1984_09 |