HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → N-cyano-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-(5-Methylimidazol-4-ylmethylthio)ethylisothiocyanate | HCID 20387426 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-cyano-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]thiourea | HCID 12918615 | 78.1% |
Reaction Steps
A solution of 2-(5-methylimidazol-4-ylmethylthio)ethylisothiocyanate [obtained from its hydrochloride (4.17 g)] in CHCl3 (20 ml) was added to a solution of cyanamide (1.05 g) and DBU (3.80 g) in CHCl3 (50 ml) and stirred overnight. After concentration, the residue was dissolved in water (30 ml) and washed with ether, decolorized with charcoal and acidified to pH 5 with 10% HCl under ice-cooling. The precipitate was filtered, washed with water and dried to give N-cyano-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]thiourea(mono-hydrate, 3.57 g). Yield 78.1%, m.p. 158°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04381395 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-441aadf59ace4f8a810f15513daa0d52 |
| Source note | uspto-grants-1983_04 |