HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248464Generated: October 25, 2026
7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid → 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(phenoxymethyl)-1-piperazinyl]-3-quinolinecarboxylic acid
https://huagongshe.com/reaction/248464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 483169 | — |
| Reactant | 3-Phenoxymethylpiperazine | HCID 19763604 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(phenoxymethyl)-1-piperazinyl]-3-quinolinecarboxylic acid | HCID 14839355 | 46.9% |
Reaction Steps
A mixture of 2 g of 3-phenoxymethylpiperazine and 701 mg of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid in 10 ml of pyridine was heated under argon in a pressure bottle at 130° C. for 18 hours. The solvents were removed and the residue chromatographed on silica gel, eluting with chloroform:methanol (9:1). The appropriate fractions were combined, evaporated, triturated with methanol and ether, then dried, giving 519 mg of the desired compound, mp 198°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05210193 |
|---|
| Source dataset | uspto-grants-1993_05 |
|---|
| ORD ID | ord-b8fee752830b4340872bb1e8ffe1ea49 |
|---|
| Source note | uspto-grants-1993_05 |
|---|