Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262387Generated: November 1, 2026

Iodoacetamide → 2-[4-(2-Fluoro-4-nitro-phenyl)-piperazin-1-yl]-acetamide

https://huagongshe.com/reaction/1262387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantAcetonitrileHCID 6342—
ReactantCesium carbonateHCID 10796—
Reactant1-(2-fluoro-4-nitrophenyl)piperazineHCID 2783066—
SolventWaterHCID 962—
Product2-[4-(2-Fluoro-4-nitro-phenyl)-piperazin-1-yl]-acetamideHCID 47184505101.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

1-(2-Fluoro-4-nitro-phenyl)-piperazine (0.438 g, 1.94 mmol), Iodoacetamide (0.401 g, 2.17 mmol), Cesium Carbonate (0.956 g, 2.93 mmol) and Acetonitrile (20 mL, 400 mmol) were combined and stirred at 60° C. for 20 hours. The mixture was cooled to room temperature. Water was added to the mixture and the product was extracted into ethyl acetate three times. The extracts were dried over sodium sulfate, filtered and concentrated to yield a yellow solid, 2-[4-(2-Fluoro-4-nitro-phenyl)-piperazin-1-yl]-acetamide (558 mg, 100%). LCMS: m/z=283.06 (M+H+); 1H NMR (400 MHz, DMSO-d6) δ 8.00 (d, 2H), 7.26 (br s, 1H), 7.17 (m, 2H), 2.94 (s, 2H), 2.60 (m, 2H), 2.50 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-ebcd69378d2643caa0fda3fdbb80ac59
Source noteuspto-grants-2013_06