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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242883Generated: October 26, 2026

Pyridine → 2-[(N,N-Dimethylamino)methyl]-6-[4-[(4-methoxybenzoyl)amino]benzyloxy]tetralin

https://huagongshe.com/reaction/1242883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantPotassium CarbonateHCID 11430—
Reactant6-(4-Aminobenzyloxy)-2-[(N,N-dimethylamino)methyl]tetralinHCID 21939722—
SolventEthyl AcetateHCID 8857—
Product2-[(N,N-Dimethylamino)methyl]-6-[4-[(4-methoxybenzoyl)amino]benzyloxy]tetralinHCID 21939788—

Reaction Steps

p-Anisoyl chloride (0.20 ml) was added dropwise to pyridine solution (6 ml) of 6-[(4-aminobenzyl)oxy]-2-[(N,N-dimethylamino)methyl]tetralin (300 mg) under ice-cooling, which was stirred at room temperature for 30 minutes. 10% aqueous potassium carbonate solution was added to the reaction mixture, and extraction was conducted using ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride solution, dried, and then concentrated. The residue was purified using alumina column chromatography (development solvent: ethyl acetate), and recrystallized (THF-IPE) to give the titled compound (300 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115750B1
Source datasetuspto-grants-2006_10
ORD IDord-bea50ce190f74682ac34c5133ddb52df
Source noteuspto-grants-2006_10