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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417969Erstellt: 26. Oktober 2026

Triethylamine → 2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPiperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2)HCID 12212341—
Edukt2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
LösungsmittelDimethylformamideHCID 6228—
ProduktAmmoniaHCID 222—
Produkt2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylateHCID 42635622158,1%

Reaktionsschritte

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 740 mg, 2.4 mmol) was dissolved in DMF (20 mL). NEt3 (1.2 mL, 8.6 mmol) and 4-(4-chlorophenyl)piperazine dihydrochloride (691 mg, 2.6 mmol) were added and the reaction mixture was stirred at room temperature for 24 hours, and the reaction mixture was then concentrated in vacuo. The resulting residue was dissolved in EtOAc (50 mL) and washed with 1M aq Na2CO3 solution (5×50 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by normal phase column chromatography (eluting with DCM, followed by a 100:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylate (696 mg, 79%) as a colourless oil which crystallized on standing to give a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093248B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-f07f9e367e1041eab2c25ceface38d43
Quellennotizuspto-grants-2012_01