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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857265Generated: November 2, 2026

4-(Aminomethyl)-N,N-dimethylaniline → HCID 22132785, compound

https://huagongshe.com/reaction/1857265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)-N,N-dimethylanilineHCID 80826—
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
Reactant4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
ProductHCID 22132785HCID 2213278515%

Reaction Steps

6,7-Dimethoxy-4-(4-aminophenoxy)quinoline (51 mg) was dissolved in toluene (5 ml) with heat, after the addition of triethylamine (1 ml), triphosgene (55 mg) was added, and the admixture was refluxed with heat for 2 minutes. (4-Dimethylaminophenyl)methylamine (104 mg) was added to the reaction mixture, and the admixture was refluxed with heat for 12 minutes. After the addition of aqueous sodium hydrogen carbonate, the reaction mixture was extracted 2 times with ethyl acetate, and the organic layer was then washed with brine and dried with anhydrous sodium sulfate. The solvent was removed by reduced-pressure distillation, and the resulting residue was purified by column chromatography on silica gel eluting with chloroform/acetone (10/1) to obtain 12 mg of the title compound (yield: 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143764
Source datasetuspto-grants-2000_11
ORD IDord-9aa1992bf0504702b6ed1c838650142d
Source noteuspto-grants-2000_11