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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162805Generated: November 3, 2026

Cyanogen Bromide → 4-(4-Fluorobenzyl)-3-oxopiperazine-1-carbonitrile

https://huagongshe.com/reaction/1162805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant1-(4-Fluorobenzyl)piperazin-2-oneHCID 18538638—
SolventDichloromethaneHCID 6344—
Product4-(4-Fluorobenzyl)-3-oxopiperazine-1-carbonitrileHCID 86074950—

Reaction Steps

To 1-(4-Fluorobenzyl)piperazin-2-one (0.50 g, 2.40 mmol, Example 1, Step 4) dissolved in methylene chloride (75 mL) was added diisopropylethylaime (0.84 mL, 4.80 mmol) and cyanogen bromide (0.28 g, 2.64 mmol) and the resultant solution was stirred overnight at room temperature. The solvent was removed in vacuo and the residue was purified by flash chromatography on silica gel using a 0-5% MeOH/CHCl3 gradient. The pure fractions were concentrated to yield the title compound as a white solid. 1H NMR (400 MHz, d6 DMSO) δ 7.31 (m, 2H), 7.18 (m, 2H), 4.54 (s, 2H), 3.98 (s, 2H), 3.49 (m, 2H), and 3.33 (m, 2H); ES MS (M+1)=234.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820680B2
Source datasetuspto-grants-2010_10
ORD IDord-54f8f30e53f34c40bc0a17937081f176
Source noteuspto-grants-2010_10