Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417977Erstellt: 26. Oktober 2026

1-Benzylpiperazine → 2-(4-Methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylate

https://huagongshe.com/reaction/417977

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BenzylpiperazineHCID 75994—
EduktDiisopropylethylamineHCID 81531—
Edukt2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-Methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylateHCID 4263579860%

Reaktionsschritte

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 567 mg, 1.8 mmol) was dissolved in DMF (15 mL). DIPEA (0.52 mL, 3.0 mmol) and 4-benzyl-piperazine (0.296 mL, 1.7 mmol) were added. The reaction mixture was stirred at room temperature for 24 hours and then concentrated in vacuo. The residue was dissolved in EtOAc (40 mL) and washed with 1 M aq Na2CO3 solution (6×50 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by reverse phase chromatography (gradient eluting with MeOH in water, 0-100%) to give 2-(4-methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylate (352 mg, 60% yield) as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093248B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-8af6a36b2aa94be18cd36b677ac064e1
Quellennotizuspto-grants-2012_01