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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379288Generated: October 30, 2026

Acetonitrile → 1-(2-Fluoro-5-pyridylmethyl) 2-(nitroimino)imidazolidine

https://huagongshe.com/reaction/379288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(Bromomethyl)-2-fluoropyridineHCID 22050638—
ReactantN-nitroimidazolidin-2-imineHCID 135413413—
SolventWaterHCID 962—
Product1-(2-Fluoro-5-pyridylmethyl) 2-(nitroimino)imidazolidineHCID 13634278850.2%

Reaction Steps

A mixture of 2-fluoro-5-pyridylmethyl bromide (9.5 g), 2-(nitroimino)imidazolidine (6.5 g), potassium carbonate (7.6 g) and acetonitrile (100 ml) was refluxed for 2 hours with stirring. After the reaction, the reaction mixture was cooled to room temperature, and cold water (100 ml) was added. The resulting crystals were collected by filtration and washed with ether to give slightly colored 1-(2-fluoro-5-pyridylmethyl)-2-(nitroimino)imidazolidine (6.0 g) as the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297374B1
Source datasetuspto-grants-2001_10
ORD IDord-1bb4a435fbe648ee83af600127f150e5
Source noteuspto-grants-2001_10