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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2204Erstellt: 23. Oktober 2026

1-(4-Pyridyl)piperazine → Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenylacetate

https://huagongshe.com/de/reaction/2204

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(4-Pyridyl)piperazineHCID 70517—
EduktBenzeneacetic acid, 4-(chloroacetyl)-, methyl esterHCID 11128026—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenylacetateHCID 18918371—

Reaktionsschritte

A solution of methyl 4-chloroacetylphenylacetate (260 mg) in acetonitrile (4 ml) was added dropwise over 15 minutes to a stirred solution of 1-(4-pyridyl)piperazine (375 mg) in acetonitrile (10 ml) and the mixture stirred overnight. The supernatent was decanted from the solid formed, concentrated in vacuo and purified by flash chromatography on neutral alumina, eluting with dichloromethane then 0.25% v/v methanol/dichloromethane and finally 0.5% v/v methanol dichloromethane. Concentration of the fractions in vacuo gave the title compound, 96 mg, as a white crystalline solid: m.p. 127°-129° C.; NMR (d6 DMSO) δ 8.15(2H,d), 7.98(2H,d), 7.41(2H,d), 6.81(2H,d), 3.91(2H,s), 3.78(2H,s), 3.53(3H,s), 3.33(4H,t), 2.64(4H,t); m/e 354(M+H )+ ; calculated for C20H23N3O3 : C, 68.0; H, 6.6; N, 11.9. found: C, 68.2; H, 6.6; N, 11.9%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728701
Quelldatensatzuspto-grants-1998_03
ORD IDord-dec26e4a500a423b998283ba15ea943b
Quellennotizuspto-grants-1998_03