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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417977Generated: October 25, 2026

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

https://huagongshe.com/reaction/417977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
SolventDimethylformamideHCID 6228—
Product2-(4-Methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylateHCID 4263579860%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-8af6a36b2aa94be18cd36b677ac064e1
Source noteuspto-grants-2012_01