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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727182Generated: October 27, 2026

1-Benzylpiperazine → 2-Methyl-3-[4-(phenylmethyl)piperazin-1-yl]quinoxaline

https://huagongshe.com/reaction/1727182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Chloro-3-methylquinoxalineHCID 236276—
ReactantSodium BicarbonateHCID 516892—
Product2-Methyl-3-[4-(phenylmethyl)piperazin-1-yl]quinoxalineHCID 36589351—

Reaction Conditions

Temperature125 °C

Reaction Steps

2-Chloro-3-methylquinoxaline (1.0 g, 5.6 mmol) and N-benzylpiperazine (2.9 ml, 16.8 mmol) were mixed and heated to 125° C. for 18 h. Saturated aqueous sodium hydrogen carbonate was added and the product was extracted with chloroform. The combined organic extracts were dried (Na2SO4) and concentrated in vacuo to give a dark red oil. The crude product was purified by flash chromatography using silica gel eluting with methanol:dichloromethane (15:85) to give the pure product as a red oil which solidified upon standing (1.63 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-820d603c06c347b0b94ae6b9ced3d67e
Source noteuspto-grants-2009_02