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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 344853Erstellt: 24. Oktober 2026

Acetic Acid → HCID 53724661, Verbindung

https://huagongshe.com/de/reaction/344853

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktWaterHCID 962—
Edukt2-(4-Fluorophenyl)piperazineHCID 4617623—
Edukt8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700554—
LösungsmittelPyridineHCID 1049—
ProduktHCID 53724661HCID 5372466146,8%

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

A suspension of 8-chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (1.6 g) and (RS)-2-(4-fluorophenyl)piperazine (3.7 g) in pyridine (16 cc) is heated to a temperature in the region of 115° C. for 24 hours. The reaction mixture is concentrated under reduced pressure (20 kPa) at approximately 60° C. The residue is taken up with ethanol (40 cc) and concentrated again under reduced pressure under the above conditions. The solid obtained is taken up with water (10 cc), treated with 10% strength acetic acid (1.75 cc), drained and washed with water (2×10 cc) and ethanol (2×10 cc). After 2 recrystallizations in dimethylformamide (10 cc each time), (RS)-7-fluoro-8-[3-(4-fluorophenyl)-1-piperazinyl]-1-methyl-4-oxo-1,4-dihydrobenzo[b ][1,8]naphthyridine-3-carboxylic acid (1.1 g) is obtained in the form of a yellow solid, m.p. 270°-275° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05053509
Quelldatensatzuspto-grants-1991_10
ORD IDord-86f51b4aa94f4fa0959685c631bcb861
Quellennotizuspto-grants-1991_10