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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16022Erstellt: 23. Oktober 2026

N,O-Dimethylhydroxylamine → N-Methoxy-N-methylquinoline-6-carboxamide

https://huagongshe.com/de/reaction/16022

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,O-DimethylhydroxylamineHCID 14232—
Edukt6-Quinolinecarboxylic acidHCID 82571—
EduktBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-Methoxy-N-methylquinoline-6-carboxamideHCID 5521117297%

Reaktionsschritte

To a solution of quinoline-6-carboxylic acid (10 g, 57.75 mmol) in DMF (200 mL) was added carbonyl diimidazole (10.3 g, 62.5 mmol) under nitrogen. The reaction was stirred for 1 hour. To the solution was added N,O-dimethyl hydroxylamine (5.6 g, 57.75 mmol), and the reaction was stirred at ambient temperature for 16 hours. The reaction was diluted with EtOAc (150 mL) and water (150 mL). The organic layer was separated, and the aqueous layer was extracted with EtOAc (5×100 mL). The organics were combined and washed with water (3×100 mL), brine (2×100 mL), dried over Na2SO4, filtered and concentrated to give quinoline-6-carboxylic acid methoxy-methyl-amide (11.97 g, 97% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732604B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-62bc40f4074643f5a8f11e7706291891
Quellennotizuspto-grants-2010_06