HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → Ethyl norfloxacin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Reactant | Ethyl 7-chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate | HCID 12733855 | — |
| Product | Ethyl norfloxacin | HCID 12733941 | 79% |
Reaction Steps
A mixture of 18 ml of picoline, 10.3 g of anhydrous piperazine, and 8.9 g of 1-ethyl-6-fluoro-7-chloro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester was refluxed with stirring for 5 hrs. The reaction mixture was concentrated under reduced pressure, and the residue was treated by the same manner described in Example 1 to give 8.2 g (79% yield) of 1-ethyl-6-fluoro-7-(1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester. mp: 178°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472579 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-d0a50ed7aa694da786f5e71445db5909 |
| Source note | uspto-grants-1984_09 |