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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1972726Erstellt: 27. Oktober 2026

Ethyl Acetate → 2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamide

https://huagongshe.com/reaction/1972726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
Edukt2-chloro-N-methylacetamideHCID 66773—
Edukt1-BenzylpiperazineHCID 75994—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamideHCID 3684523083%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 1-benzyl-piperazine (1.0 g, 5.67 mmol), 2-chloro-N-methylacetamide (671.2 mg, 6.24 mmol, 1.1 eq.), and potassium carbonate (941 mg, 6.81 mmol, 1.2 eq.) in anhydrous THF (23 mL) was stirred at 60° C. under N2 for 18 h. The mixture was cooled to rt and poured into EtOAc. The organic phase was washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by MPLC (Biotage®, gradient elution 1:4:5 v/v MeOH:Acetone:DCM) to give 1.16 g (83%) of the product as a white solid. 1H-NMR (300 MHz, DMSO-d6) 7.62 to 7.56 (broad d, 1H), 7.33 to 7.20 (m, 5H), 3.45 (s, 2H), 2.85 (s, 2H), 2.58 (d, 3H), 2.44 to 2.33 (broad s, 8H); ES-MS m/z 248.2 [M+H]+, RT (min) 0.33.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08431695B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-3cf0cccfa4de48788a451027f19e9182
Quellennotizuspto-grants-2013_04