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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387807Generated: October 25, 2026

3-Ethylpyridine → 3-Ethyl-1-[4-(7-phenyl-3,4-dihydronaphthalene-2-carboxamido)benzyl]pyridinium chloride

https://huagongshe.com/reaction/1387807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-EthylpyridineHCID 10823—
ReactantN-[4-(chloromethyl)phenyl]-7-phenyl-3,4-dihydronaphthalene-2-carboxamideHCID 10809385—
SolventDimethylformamideHCID 6228—
Product3-Ethyl-1-[4-(7-phenyl-3,4-dihydronaphthalene-2-carboxamido)benzyl]pyridinium chlorideHCID 18472572—

Reaction Conditions

Temperature70 °C

Reaction Steps

In DMF (3 ml) was dissolved N-[4-(chloromethyl)-phenyl]-7-phenyl-3,4-dihydronaphthalene-2-carboxamide (160 mg), and to the mixture was added 3-ethylpyridine (146 μl). The mixture was stirred at 70° C. for 72 hours and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-methanol to give 3-ethyl-1-[4-(7-phenyl-3,4-dihydronaphthalene-2-carboxamido)benzyl]pyridinium chloride (Compound 27) (185 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-4cae7f802b1f43ceb0594a0fd2589469
Source noteuspto-grants-2001_07