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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 648511Erstellt: 24. Oktober 2026

4-Aminobenzoic Acid → 4-[[3-Ethoxycarbonyl-7-(trifluoromethyl)-4-quinolyl]amino]benzoic acid hydrochloride

https://huagongshe.com/de/reaction/648511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Aminobenzoic AcidHCID 978—
EduktEthyl 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylateHCID 14515676—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[[3-Ethoxycarbonyl-7-(trifluoromethyl)-4-quinolyl]amino]benzoic acid hydrochlorideHCID 1382503561,1%

Reaktionsschritte

A mixture of ethyl 4-chloro-7-(trifluoromethyl)-3-quinoline-carboxylate (3.04 g) and 4-aminobenzoic acid (1.37 g) in tetrahydrofuran (53 ml) was stirred under reflux for 10 hours and cooled to room temperature. The precipitates were collected and washed with tetrahydrofuran to give 4-[[3-ethoxycarbonyl-7-(trifluoromethyl)-4-quinolyl]amino]benzoic acid hydrochloride (2.69 g) as yellow powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04735952
Quelldatensatzuspto-grants-1988_04
ORD IDord-bebe478147bd4c42b33c1475c46188a7
Quellennotizuspto-grants-1988_04