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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162801Generated: October 28, 2026

Methyl iodide → 1-{[4-(4-fluorobenzyl)-3-oxopiperazin-1-yl]carbonyl}-3-methyl-1H-imidazol-3-ium iodide

https://huagongshe.com/reaction/1162801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-(4-fluorobenzyl)-4-(1H-imidazol-1-ylcarbonyl)piperazin-2-oneHCID 68432812—
SolventAcetonitrileHCID 6342—
SolventAluminumHCID 5359268—
Product1-{[4-(4-fluorobenzyl)-3-oxopiperazin-1-yl]carbonyl}-3-methyl-1H-imidazol-3-ium iodideHCID 86617471—

Reaction Steps

To a solution of 1-(4-fluorobenzyl)-4-(1H-imidazol-1-ylcarbonyl)piperazin-2-one (2.49 g, 8.2 mmol) in 20 mL of anhydrous MeCN, under an atmosphere of nitrogen, was added iodomethane (2.05 mL, 32.9 mmol). The reaction was covered in aluminum foil and stirred at room temperature overnight. The reaction was concentrated under vacuum, co-evaporated with toluene under vacuum, followed by drying under high vacuum to provide the title compound. 1H NMR (400 MHz, DMSO-d6) δ 9.59 (s, 1H), 8.02 (s, 1H), 7.84 (s, 1H), 7.36 (dd, J=8.4, 5.7 Hz, 2H), 7.19 (t, J=8.7 Hz, 2H), 4.56 (s, 2H), 4.23 (s, 2H), 3.91 (s, 3H), 3.77 (bs, 2H), 3.40 (t, J=5.2 Hz, 2H). ES MS (M)=317.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820680B2
Source datasetuspto-grants-2010_10
ORD IDord-550d62e398c84da1a882326c90d9596f
Source noteuspto-grants-2010_10