N,N'-Dimethylurea → HCID 178485109, compound

Participants

Reaction Steps

Phosphoryl chloride (4.4 ml, 0.047M) was added with cooling to dimethylurea (4 g, 0.045M) in tetrahydrofuran (60 ml). After stirring at room temperature for 5 hours the mixture was added to 2-(4-amino-2,6-dichlorophenylimino)imidazolidine (3.0 g, 0.012M) in tetrahydrofuran (60 ml). The mixture was refluxed for 18 hours and then evaporated to give an oily solid. The residue was extracted into 2M HCl, washed with methylene chloride and then basified. Extraction of the alkaline mixture with methyl chloride yielded a gum on evaporation of the extract. The gum was taken up in ethanol and the required guanidino compound (300 mg) crystallised. The product was recrystallised as 2-[2,6-dichloro-4-(1,3-dimethylguanidino)phenylimino]imidazolidine dihydroiodide (MP 320° C.).

Provenance & Evidence