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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14240Erstellt: 24. Oktober 2026

Triethylamine → Methyl quinoline-7-carboxylate

https://huagongshe.com/de/reaction/14240

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktQuinolin-7-yl trifluoroacetateHCID 21087171—
EduktN,N-dimethylformamide methanolHCID 21901440—
ProduktMethyl quinoline-7-carboxylateHCID 12554532—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a stirred solution of quinolin-7-yl trifluoroacetate (750 mg, 2.7 mmol), PdCl2(Ph3P) (95 mg, 0.14 mmol), and triethylamine (1.2 mL, 8.4 mmol) in 1:2 DMF/MeOH (39 mL) was degassed and sparged with CO, and the mixture was heated at 60° C. for 48 h. The mixture was cooled to room temperature, filtered through diatomaceous earth, and concentrated under reduced pressure. The residue was diluted with a 5% solution of LiCl, and washed with CHCl3 (3×250 mL). The combined organics were dried (Na2SO4), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 3:1 ethyl acetate/hexanes) provided methyl quinoline-7-carboxylate (185 mg): ESI MS m/z 188 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-80f411743c6a47c7bbddd39f6e9301b5
Quellennotizuspto-grants-2010_06