Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413472Generated: October 26, 2026

Potassium Carbonate → 1-(2-Chloro-5-methyl-3-pyridylmethyl)2-nitroiminoimidazolidine

https://huagongshe.com/reaction/413472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCesium ChlorideHCID 24293—
Reactant2-Chloro-3-(chloromethyl)-5-methylpyridineHCID 11206082—
ReactantN-nitroimidazolidin-2-imineHCID 135413413—
SolventAcetonitrileHCID 6342—
Product1-(2-Chloro-5-methyl-3-pyridylmethyl)2-nitroiminoimidazolidineHCID 13634771290%

Reaction Steps

2-chloro-3-chloromethyl-5-methylpyridine (1.3 g, 0.0076 moles) was added to a well-stirred material comprising of 2-nitroimino-1, 3-diazacyclopentane (1.18 g, 0.00912 moles), potassium carbonate (1.16 g, 0.0083 moles), cesium chloride (0.04 g, 0.00024 moles) in acetonitrile (10 ml) solvent at room temperature. The reaction mixture was refluxed for 5 hours. Solvent was removed under reduced pressure and the mass diluted with water (25 ml). The mass was then extracted with methylene chloride (2×50 ml) and the layers were separated. Organic layer was dried over sodium sulphate and solvent removed under reduced pressure. The residue obtained was subjected to chromatographic purification on silica gel to give 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimidazolidine in 90% yield. NMR (CDCl3+DMSO d6): δ2.38 (s, 3H, CH3), 3.58 (t, 2H, N—CH2), 3.74 (t, 2H, N—CH2), 4.52 (s, 2H, CH2), 7.54 (s, 1H, aromatic), 812 (s, 1H, aromatic), 8.86 (1H, NH). Mass: M+. 269.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566528B1
Source datasetuspto-grants-2003_05
ORD IDord-7586f01012af4ed18c167210e9a16ebd
Source noteuspto-grants-2003_05