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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296650Generated: October 30, 2026

Piperazine → 2-[1-(2-Methoxyphenyl)ethoxy]-6-(1-piperazinyl)pyrazine

https://huagongshe.com/reaction/1296650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18186880HCID 18186880—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product2-[1-(2-Methoxyphenyl)ethoxy]-6-(1-piperazinyl)pyrazineHCID 1818693067%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of the product from step 1 above (0.93 g, 3.53 mmol) piperazine (0.88 g, 10.2 mmol) and K2CO3 (0.49 g, 3.53 mmol) in acetonitrile (7 mL) was heated in a sealed pyrex flask at 90° C. for 6.5 h. The reaction mixture was diluted with dichloromethane, filtered and concentrated in vacuo. The semi-solid residue was purified by silica gel chromatography (13×4 cm) using CHCl3/MeOH (9:1) as eluent. Solvents were evaporated off and the remaining oil was redissolved in CHCl3, filtered through a short plug of alumina, covered with K2CO3, using CHCl3 as eluent. Solvent removal in vacuo gave 0.74 g (67%) of the title compound as a beige oil. HRMS m/z calcd for C17H22N4O2 (M)+ 314.1743, found 314.1733. Anal. (C17H22N4O2.0.5H2O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247633B2
Source datasetuspto-grants-2007_07
ORD IDord-f874605d6d204a1f86b765c62fbc3b2a
Source noteuspto-grants-2007_07