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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295724Generated: October 26, 2026

Benzyl Bromide → 3-(4-Benzylpiperazin-1-yl)-1-[2-(2,4,5-trifluorophenoxy)ethyl]pyrazin-2(1H)-one hydrochloride

https://huagongshe.com/reaction/1295724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant2(1H)-Pyrazinone, 3-(1-piperazinyl)-1-[2-(2,4,5-trifluorophenoxy)ethyl]-HCID 10405848—
Reactant3-(1-Piperazinyl)-1-[2-(2,4,5-trifluorophenoxy)ethyl]-2(1H)-pyrazinone, HydrochlorideHCID 11639709—
Product3-(4-Benzylpiperazin-1-yl)-1-[2-(2,4,5-trifluorophenoxy)ethyl]pyrazin-2(1H)-one hydrochlorideHCID 10435302—

Reaction Steps

The title compound was prepared according to the procedure of Example 60 starting from 3-(1-piperazinyl)-1-[2-(2,4,5-trifluorophenoxy)ethyl]-2(1H)-pyrazinone (0.35 g, 1.0 mmol; from the free base of Example 3) and benzyl bromide (0.19 g, 1.1 mmol) Yield: 0.17 g (35%); HPLC purity: 99%; mp 214-214.5° C. HRMS calc for C23H23F3N4O2 (M)+ 444.1773, found 444.1789.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244722B2
Source datasetuspto-grants-2007_07
ORD IDord-33b9381be5ad40ca9f2e1fe044a466b6
Source noteuspto-grants-2007_07