Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928766Generated: November 1, 2026

Hydrochloric Acid → 3-Benzyl-N-methoxy-N,2,4-trimethylquinoline-6-carboxamide

https://huagongshe.com/reaction/928766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,O-DimethylhydroxylamineHCID 14232—
ReactantEthyl 3-benzyl-2,4-dimethylquinoline-6-carboxylateHCID 86715607—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyl-N-methoxy-N,2,4-trimethylquinoline-6-carboxamideHCID 86715609—

Reaction Steps

A slurry of ethyl 3-benzyl-2,4-dimethylquinoline-6-carboxylate (99.5 mg, 0.312 mmol, Intermediate 34: step b) and N,O-dimethylhydroxylamine.HCl (42.2 mg, 0.433 mmol) in THF (1 mL) was stirred at 0° C. under argon while iPrMgCl (2.01 M in THF, 0.43 mL, 0.864 mmol) was added dropwise. The resulting dark solution was stirred at 0° C. overnight while the ice bath expired. It was then quenched with 5 M aqueous NH4Cl (4 mL) and extracted with EtOAc (2×3 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated, and the residue was flash chromatographed with a heptane to 100% EtOAc gradient to yield the title compound as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290476B2
Source datasetuspto-grants-2016_03
ORD IDord-ff59fc8934594befa2d462f531d46883
Source noteuspto-grants-2016_03