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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417975Generated: October 26, 2026

Diisopropylethylamine → 2-(4-Methyl-piperazin-1-yl)ethyl 4-(4-methoxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-Methoxyphenyl)piperazineHCID 269722—
Reactant2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
SolventDimethylformamideHCID 6228—
Product2-(4-Methyl-piperazin-1-yl)ethyl 4-(4-methoxyphenyl)piperazine-1-carboxylateHCID 4263579617.2%

Reaction Steps

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 680 mg, 2.2 mmol) was dissolved in DMF (20 mL). DIPEA (0.76 mL, 4.4 mmol) and 4-(4-methoxyphenyl)piperazine (422 mg, 2.2 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 residue was purified by normal phase column chromatography (eluting with DCM, followed by a 500:8:1 mixture of DCM:EtOH:NH3, followed by a 50:8:1 mixture of DCM:EtOH:NH3). The residue was recrystallised from EtOAc to give 2-(4-methyl-piperazin-1-yl)ethyl 4-(4-methoxyphenyl)piperazine-1-carboxylate (137 mg, 17%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-4ad1924324954db0ae1cccaf247fd855
Source noteuspto-grants-2012_01