HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544410Generated: October 31, 2026
N,N'-Dimethylurea → HCID 178485109, compound
https://huagongshe.com/reaction/544410
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylurea | HCID 7293 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178507681 | HCID 178507681 | — |
| Product | HCID 178485109 | HCID 178485109 | — |
Reaction Steps
Phosphoryl chloride (4.4 ml, 0.047 M) was added with cooling to dimethylurea (4 g, 0.045 M) 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, 0.012 M) in tetrahydrofuran (60 ml). The mixture was refluxed for 18 hours and then evaporated to give an oily solid. The residue was extracted into 2 M 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450170 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-1996bd2f1fef479da406c1abfca3b17a |
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| Source note | uspto-grants-1984_05 |
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