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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878390Generated: November 2, 2026

Sodium Iodide → N-tert-Butyl-3-((4-(3-fluoro-4-nitrobenzoyl)-2-(fluoromethyl)piperazin-1-yl)methyl)benzamide

https://huagongshe.com/reaction/1878390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantN-tert-butyl-3-(chloromethyl)benzamideHCID 43156221—
Reactant(3-Fluoro-4-nitrophenyl)(3-(fluoromethyl)piperazin-1-yl)methanoneHCID 66878536—
SolventAcetonitrileHCID 6342—
ProductN-tert-Butyl-3-((4-(3-fluoro-4-nitrobenzoyl)-2-(fluoromethyl)piperazin-1-yl)methyl)benzamideHCID 5791772257.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A stirred mixture of (3-fluoro-4-nitrophenyl)(3-(fluoromethyl)piperazin-1-yl)methanone (456 mg, 1.6 mmol), N-tert-butyl-3-(chloromethyl)benzamide (361 mg, 1.6 mmol), triethylamine (3.1 mmol, 341 mg) and sodium iodide (1.6 mmol, 240 mg) in acetonitrile (10 mL) was heated to 60° C. for several hours. The reaction was concentrated under reduced pressure. The residue was then dissolved in dichloromethane and extracted with water (×3). The organic phase was dried (sodium sulfate) and concentrated under vacuum. The crude material was purified using silica chromatography to give the title compound (435 mg). MS (ESI) m/z 475.7[M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-736fb81fe7f04add9513906cdd091f46
Source noteuspto-grants-2012_11