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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266740Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/266740

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.; (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 C21H25N3O4 : 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
PatentnummerUS05652242
Quelldatensatzuspto-grants-1997_07
ORD IDord-2be04a7ca45447cfba0de30476c8ee08
Quellennotizuspto-grants-1997_07