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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2218Erstellt: 23. Oktober 2026

1-(4-Pyridyl)piperazine → Ethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetate

https://huagongshe.com/de/reaction/2218

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(4-Pyridyl)piperazineHCID 70517—
EduktEthyl 2-[4-(2-bromoacetyl)phenoxy]acetateHCID 18408936—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetateHCID 18918266—

Reaktionsschritte

Ethyl 4-bromoacetylphenoxyacetate (6.0 g) was added to a stirred, cooled (4° C.) solution of 1-(4-pyridyl)piperazine (6.5 g) in acetonitrile (225 ml). Stirring was continued for 1 hour at 4° C., then overnight at ambient temperature when the precipitated solid was removed by filtration. The filtrate was evaporated in vacuo and the solid residue triturated with water, filtered, then washed with water and dried. Recrystallisation from a small volume of ethanol gave the title compound, 1.71 g, as a cream coloured solid: m.p. 113°-114° C.; NMR (d6DMSO) δ 8.15 (2H, d), 7.98 (2H, d), 7.02 (2H, d), 6.80 (2H, d), 4.89 (2H, d), 4.17 (2H, q), 3.84 (2H, s), 3.32 (4H, t), 2.62 (4H, t), 1.22 (3H, t); m/e 384 (M+H)+ ; calculated for C21H25 N3O4 : C, 65.8; H, 6.6; N, 11.0. found: C, 65.5; H, 6.6; N, 10.8%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728701
Quelldatensatzuspto-grants-1998_03
ORD IDord-f92e4a744b9845aba8f9beb80f6700fd
Quellennotizuspto-grants-1998_03