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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445022Generated: October 29, 2026

Sodium Iodide → Dpi-221

https://huagongshe.com/reaction/445022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant3-Fluorobenzyl bromideHCID 68007—
Reactant[Bromo(fluoro)methyl]benzeneHCID 316418—
Reactant4-((alpha-s)-alpha-((2s,5r)-2,5-Dimethyl-1-piperazinyl)benzyl)-n,n-diethylbenzamideHCID 10215864—
SolventAcetonitrileHCID 6342—
ProductDpi-221HCID 9891642—

Reaction Steps

A solution of 4-((alpha-S)-alpha-((2S,5R)-2,5-dimethyl-1-piperazinyl)benzyl)-N,N-diethylbenzamide (9.128 g, 24.05 mmol) in acetonitrile (150 mL) was added to sodium iodide (360 mg, 2.4 mmol) and stirred under nitrogen during the addition of triethylamine (12 mL, 8.76 g, 86.6 mmol), followed by 3-fluorobenzyl bromide (5.9 mL, 9.09 g, 48.1 mmol). An immediate turbidity was observed on addition of the fluorobenzyl bromide, thickening to a white crystalline precipitate over one hour. The reaction mixture was stirred under nitrogen overnight at room temperature. The solvent was removed by evaporation, and saturated sodium bicarbonate solution (25 mL) was added to the residue. The copious white precipitate was collected by filtration, washed well with water and dried under vacuum at room temperature. (10.54 g, 89.2%). Calc. for C31H38FN3O 0.2 H2O: C, 75.79; H, 7.88; N, 8.55; F, 3.87. Found C, 75.80; H, 7.78; N, 8.49; F, 3.75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476280B2
Source datasetuspto-grants-2013_07
ORD IDord-d57cb1431af5487a8ec7ab2830986001
Source noteuspto-grants-2013_07