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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417971Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/417971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-(o-Tolyl)piperazine dihydrochlorideHCID 91964—
Edukt2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
LösungsmittelDimethylformamideHCID 6228—
ProduktAmmoniaHCID 222—
Produkt2-(4-Methylpiperazin-1-yl)-ethyl 4-(2-methylphenyl)piperazine-1-carboxylateHCID 4263562563,5%

Reaktionsschritte

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 866 mg, 2.8 mmol) was dissolved in DMF (20 mL). NEt3 (1.5 mL, 10.8 mmol) and 4-(2-methyl-phenyl)piperazine dihydrochloride (704 mg, 2.8 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 1 M 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 200:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)-ethyl 4-(2-methylphenyl)piperazine-1-carboxylate (308 mg, 32%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093248B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-c0c8dd23ff8445d6b7dbdd024fa46b42
Quellennotizuspto-grants-2012_01