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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417970Generated: October 26, 2026

1-(3-(Trifluoromethyl)phenyl)piperazine → 2-(4-Methylpiperazin-1-yl)ethyl 4-(3-trifluoromethyl-phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
ReactantTriethylamineHCID 8471—
Reactant2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
Product2-(4-Methylpiperazin-1-yl)ethyl 4-(3-trifluoromethyl-phenyl)piperazine-1-carboxylateHCID 42635623126.1%

Reaction Steps

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 761 mg, 2.5 mmol) was dissolved in DMF (20 mL). NEt3 (0.4 mL, 2.9 mmol) and 4-(3-trifluoromethyl-phenyl)piperazine (583 mg, 2.5 mmol) were added and the reaction mixture was stirred at room temperature for 24 hours, 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 100:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)ethyl 4-(3-trifluoromethyl-phenyl)piperazine-1-carboxylate (631 mg, 64%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-8139c60e46dd481ba056a1403dd7669b
Source noteuspto-grants-2012_01