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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493330Generated: October 30, 2026

Diphenyl Ether → 4-Benzyl-1-(3-chloro-2-pyrazinyl)-cis-2,6-dimethylpiperazine

https://huagongshe.com/reaction/493330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl EtherHCID 7583—
ReactantTributylamineHCID 7622—
Reactant2,3-DichloropyrazineHCID 78575—
Reactant(3r,5s)-1-Benzyl-3,5-dimethylpiperazineHCID 12197174—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-Benzyl-1-(3-chloro-2-pyrazinyl)-cis-2,6-dimethylpiperazineHCID 53660138—

Reaction Conditions

Temperature220 °C

Reaction Steps

A mixture of 2,3-dichloropyrazine (4.9 g, 32.9 mmol), 1-benzyl-cis-3,5-dimethylpiperazine (5.9 g, 29.0 mmol), tributylamine (5.9 g, 32 mmol) and diphenyl ether (70 mL) was heated in a sealed tube at 220° C. for 3 days. The reaction mixture was cooled to ambient temperature and EtOAc (200 mL) and toluene (100 mL) were added. The organic phase was extracted with 5 M aqueous HCl (×3) and the combined aqueous phases were extracted with CHCl3 (×3). The combined organic layers, which contained the product, were washed with aqueous NaOH (5 M), dried (MgSO4), and the solvent was evaporated. The crude product (0.96 g), about 80% pure based on GC, was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534794B2
Source datasetuspto-grants-2009_05
ORD IDord-70452dfa31b140209022565b4cb90eb8
Source noteuspto-grants-2009_05