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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245159Erstellt: 23. Oktober 2026

2-Oxobutanoic Acid → 6-Fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/de/reaction/245159

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Oxobutanoic AcidHCID 58—
Edukt3-(Trifluoromethyl)benzaldehydeHCID 67990—
Edukt4-Fluoro-3-methoxyanilineHCID 2774533—
LösungsmittelEthanolHCID 702—
Produkt6-Fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 6738400253%

Reaktionsschritte

A solution of the 4-fluoro-3-(methyloxy)aniline (11.29 g, 80 mmol) and 3-(trifluoromethyl)benzaldehyde (13.93 g, 80 mmol) in ethanol (200 mL) was heated to reflux for 1 h. 2-Oxobutanoic acid (8.17 g, 80 mmol) was added portionwise. The reaction mixture was stirred at reflux for additional 3 h, cooled to room temperature, and stirred at room temperature overnight. The solid was collected by filtration, washed with ethanol, and air dried to give 6-fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (16.05 g, 53% yield). 1H NMR (400 MHz, DMSO-d6) δ 14.35 (br. s., 1H), 7.93-8.00 (m, 2H), 7.85-7.91 (m, J=7.78 Hz, 1H), 7.74-7.81 (m, 1H), 7.68-7.73 (m, J=8.53 Hz, 1H), 7.54 (d, J=12.05 Hz, 1H), 4.03 (s, 3H), 2.38 (s, 3H); MS (m/z) 380.1 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658636B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-3208982a3586496eb304f0992840799f
Quellennotizuspto-grants-2014_02