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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408084Generated: November 1, 2026

Morpholine → 8-Quinolinecarboxylic acid, 6-fluoro-1,2,3,4-tetrahydro-4,4-dimethyl-2-[3-(4-morpholinyl)phenyl]-

https://huagongshe.com/reaction/2408084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-Dimethylglycine hydrochlorideHCID 75605—
ReactantHCID 70496195HCID 70496195—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product8-Quinolinecarboxylic acid, 6-fluoro-1,2,3,4-tetrahydro-4,4-dimethyl-2-[3-(4-morpholinyl)phenyl]-HCID 7049742061.4%

Reaction Steps

A mixture solution of 2-(3-bromo-phenyl)-6-fluoro-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester (5 g, 12.7 mmol), morpholine (11.1 mL, 125 mmol), copper(I) iodide (1.43 g, 7.5 mmol), N,N-dimethylglycine hydrochloride (1.4 g, 10 mmol), and potassium carbonate (5.2 g, 75 mmol) in dimethyl sulfoxide (20 mL) was stirred at 120° C. for 16 h. Then the reaction mixture was cooled to room temperature. The reaction mixture was extracted with ethyl acetate (150 mL×2), washed with saturated aqueous ammonium chloride solution (50 mL×3) and brine (50 mL×2), dried over anhydrous sodium sulfate and then concentrated in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 30-50% ethyl acetate in petroleum ether) to afford 6-fluoro-4,4-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid (3 g, 61%) as a white solid: MS (ESI) M+1=385.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-6280aa0660a24076aa727036e2d482b0
Source noteuspto-grants-2014_08