HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Methylpiperazine → rac-1-Ethyl-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinoline-carboxylic acid monosodium salt
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Methylpiperazine | HCID 66057 | — |
| Edukt | 7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 483169 | — |
| Edukt | Sodium 2-ethylhexanoate | HCID 23672331 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | rac-1-Ethyl-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinoline-carboxylic acid monosodium salt | HCID 67896247 | 75% |
Reaktionsschritte
A mixture of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid [J. Med. Chem., 23, 1358 (1980)] (0.52 g, 2 mmol) and 2-methylpiperazine (0.8 g, 8 mmol) was heated at 175° for 5 hours. The residue was dissolved in ethylacetate (10 mL) and chloroform (10 mL), and a solution of sodium-2-ethyl- hexanoate (0.33 g, 2 mmol) in ethyl acetate (20 mL) was added. The mixture was stirred for 30 minutes and the precipitate was collected. The crude product was purified by preparative liquid chromatography (C-18 reverse phase, gradient 0-40% acetonitrile in water) to give a pale yellow lyophilized solid (0.5 g, 75% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05162523 |
| Quelldatensatz | uspto-grants-1992_11 |
| ORD ID | ord-f139f0669db54306a99a6acbf3f14bfb |
| Quellennotiz | uspto-grants-1992_11 |