HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 1-(2-Fluoro-5-pyridylmethyl) 2-(nitroimino)imidazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(Bromomethyl)-2-fluoropyridine | HCID 22050638 | — |
| Reactant | N-nitroimidazolidin-2-imine | HCID 135413413 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Fluoro-5-pyridylmethyl) 2-(nitroimino)imidazolidine | HCID 136342788 | 50.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428032 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-ebb2b9f9fe42400aa8d3315b4666b29b |
| Source note | uspto-grants-1995_06 |