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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16022Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,O-DimethylhydroxylamineHCID 14232—
Reactant6-Quinolinecarboxylic acidHCID 82571—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-Methoxy-N-methylquinoline-6-carboxamideHCID 5521117297%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732604B2
Source datasetuspto-grants-2010_06
ORD IDord-62bc40f4074643f5a8f11e7706291891
Source noteuspto-grants-2010_06