Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1035286Erstellt: 25. Oktober 2026

Benzathine → Ethyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylate

https://huagongshe.com/reaction/1035286

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzathineHCID 8793—
EduktDiethyl bromomalonateHCID 69637—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelSodium HydroxideHCID 14798—
ProduktEthyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylateHCID 15645950—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of N,N′-dibenzylethylenediamine (14.12 mL, 60.2 mmol) in acetonitrile (100 mL) was added diethyl bromomalonate (5.14 mL, 30.1 mmol), and the mixture was heated with an oil bath at 90° C. (reflux) for 7 hours. The solvent was evaporated to provide a residue that was dissolved in 1 M NaOH (aqueous), and the mixture was extracted with ethyl acetate twice, dried over Na2SO4, and the solvent was evaporated. The crude mixture was purified by silica gel chromatography (Analogix IntelliFlash 280, SF40-150) eluting with 15%-30% ethyl acetate/hexanes to afford the title compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.38-7.20 (m, 10H), 4.54 (dd, J=15.0, 154.2, 2H), 4.20-4.10 (m, 2H), 4.03 (q, J=7.1, 1H), 3.96 (s, 1H), 3.61 (dd, J=13.5, 41.7, 2H), 3.27-3.14 (m, 2H), 3.05-2.95 (m, 1H), 2.60-2.52 (m, 1H), 1.23 (t, J=7.1, 3H); MS (ESI+) m/z 353.0 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08546377B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-f8dff528f719486c8df628f1de96d9a3
Quellennotizuspto-grants-2013_10