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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417969Generated: October 26, 2026

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

https://huagongshe.com/reaction/417969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2)HCID 12212341—
Reactant2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
Product2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylateHCID 42635622158.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-f07f9e367e1041eab2c25ceface38d43
Source noteuspto-grants-2012_01