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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359506Generated: October 30, 2026

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

https://huagongshe.com/reaction/359506

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 numberUS05001138
Source datasetuspto-grants-1991_03
ORD IDord-8f03afa67c5c4f73a53c530329a84329
Source noteuspto-grants-1991_03