HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanamide → HCID 178512333, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | HCID 178468268 | HCID 178468268 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178512333 | HCID 178512333 | 72.1% |
Reaction Steps
To 1.9 g of ethyl 3-[(2-guanidinothiazol-4-yl)methylthio]-propionimidate was added 10 ml of an ethanol solution of 0.28 g of cyanamide and the mixture was allowed to stand overnight at room temperature. Then, the solvent was distilled off from the reaction mixture under reduced pressure and the residue obtained was purified by a silica gel column chromatography using a solvent mixture of chloroform and methanol as a developing solvent to provide 1.35 g of N-cyano-3-[(2-guanidinothiazol-4-yl)methylthio]propionamidine. The product shows the following physicochemical properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04362736 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-57d2764e71aa4168a95641ad79475e36 |
| Source note | uspto-grants-1982_12 |