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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228083Generated: October 30, 2026

1-Methylpiperazine → HCID 18472616, compound

https://huagongshe.com/reaction/2228083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[4-(chloromethyl)phenyl]-7-(4-methylphenyl)-3,4-dihydronaphthalene-2-carboxamideHCID 18472361—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18472616HCID 18472616—

Reaction Steps

In THF (7 ml) was dissolved N-[4—(chloromethyl)-phenyl]-7—(4-methylphenyl)-3,4-dihydro-naphthalene-2-carboxamide (150 mg), and to the mixture was added 1-methylpiperazine (129 μl). The mixture was refluxed for 24 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=20/1) and recrystallized from ethyl acetate-hexane to give 7—(4-methylphenyl)-N-[4—(4-methyl-1-piperazinylmethyl)phenyl]-3,4-dihydronaphthalene-2-carboxamide (Compound 40) (105 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-fbc0d1dea1c944048d777b14f0caf6b6
Source noteuspto-grants-2002_07