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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417973Generated: October 31, 2026

Triethylamine → HCID 42635793, compound

https://huagongshe.com/reaction/417973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(2,5-Xylyl)piperazineHCID 70542—
Reactant2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
ProductHCID 42635793HCID 4263579354.3%

Reaction Steps

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 866 mg, 2.8 mmol) was dissolved in DMF (25 mL). NEt3 (0.5 mL, 3.6 mmol) and 4-(2,5-dimethyl-phenyl)piperazine (580 mg, 3.1 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 200:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)ethyl 4-(2,5-dimethyl-phenyl)piperazine-1-carboxylate (274 mg, 27%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-eb981d6429644a3381b83f69fdadd97b
Source noteuspto-grants-2012_01