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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228089Generated: October 29, 2026

1-(2-Hydroxyethyl)piperazine → HCID 54426903, compound

https://huagongshe.com/reaction/2228089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[4-(chloromethyl)phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamideHCID 18472361—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54426903HCID 54426903—

Reaction Steps

In THF (7 ml) was dissolved N-[4—(chloromethyl)-phenyl]-7—(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamide (150 mg), and to the mixture was added 1—(2-hydroxyethyl)piperazine (14 μl). The mixture was refluxed for 22 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 recrystallized from ethyl acetate-hexane to give N-[4-[1—(2-hydroxyethyl)-4-piperazinylmethyl]phenyl]-7—(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamide (Compound 46) (158 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-1970d073e3fd46e3a11cbf83a268f918
Source noteuspto-grants-2002_07