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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1387807Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1387807

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-EthylpyridineHCID 10823—
EduktN-[4-(chloromethyl)phenyl]-7-phenyl-3,4-dihydronaphthalene-2-carboxamideHCID 10809385—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Ethyl-1-[4-(7-phenyl-3,4-dihydronaphthalene-2-carboxamido)benzyl]pyridinium chlorideHCID 18472572—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06268354B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-4cae7f802b1f43ceb0594a0fd2589469
Quellennotizuspto-grants-2001_07