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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277074Generated: November 1, 2026

Diethanolamine → N-[4-[N,N-bis(2-hydroxyethyl)-aminomethyl]phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamide

https://huagongshe.com/reaction/1277074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethanolamineHCID 8113—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[4-(chloromethyl)phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamideHCID 18472361—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-[N,N-bis(2-hydroxyethyl)-aminomethyl]phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamideHCID 18472290—

Reaction Steps

In THF (10 ml) was dissolved N-[4-(chloromethyl)-phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamide (300 mg), and to the mixture was added diethanolamine (222 μl). The mixture was refluxed for 34 hours. The reaction mixture was cooled to room temperature, and to the mixture was added 5% sodium hydrogen carbonate solution (50 ml). The mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/triethylamine=10/1) and recrystallized from ethyl acetate-hexane to give N-[4-[N,N-bis(2-hydroxyethyl)aminomethy]phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamide (Compound 51) (148 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-1538b7a2cf594bdeabfee1095625ac63
Source noteuspto-grants-2000_12