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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417968Erstellt: 26. Oktober 2026

1-Phenylpiperazine → 2-(4-Methyl-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate formate

https://huagongshe.com/reaction/417968

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-PhenylpiperazineHCID 7096—
EduktDiisopropylethylamineHCID 81531—
Edukt2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(4-Methyl-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate formateHCID 6665098811,7%

Reaktionsschritte

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 1.58 g, 5.1 mmol) was dissolved in DMF (25 mL). DIPEA (0.87 mL, 5.0 mmol) and 4-phenyl-piperazine (807 mg, 0.76 mL, 5.0 mmol) were added and the reaction mixture was stirred at room temperature for 14 hours. The reaction mixture was then concentrated in vacuo. The residue was purified by reverse phase column chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-100%) to give 2-(4-methyl-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate formate (113 mg, 6.7%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093248B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-e3baaee6b1f2426fad3952ca369662ae
Quellennotizuspto-grants-2012_01