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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231174Generated: October 31, 2026

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

https://huagongshe.com/reaction/231174

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 numberUS04845106
Source datasetuspto-grants-1989_07
ORD IDord-d7497918dae34e8ea8fd1994f5ff733e
Source noteuspto-grants-1989_07