HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → N-Cyano-N'-propargyl-N"-(2-mercaptoethyl)guanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Carbamimidothioic acid, N-cyano-N'-2-propynyl-, methyl ester | HCID 2805748 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Cyano-N'-propargyl-N"-(2-mercaptoethyl)guanidine | HCID 136182246 | — |
Reaction Steps
A mixture of the product of Step A of Example 5 (1.53 g; 10 mmoles), cysteamine hydrochloride (1.136 g; 10 mmoles) and 0.055 g of hydroquinone in 10 ml of dimethylformamide is slightly warmed to dissolve. To this solution is added 10 ml of 1 N aqueous sodium hydroxide and nitrogen is bubbled through the solution. After standing at room temperature for 17 hours, the reaction mixture is evaporated to dryness to give a mixture of the title compound and sodium chloride. The title compound is extracted from the mixture with 10 ml of ethanol and the ethanolic solution is used in Step B below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282363 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-f9d81d1b4cfc4966b3d434ca206e909c |
| Source note | uspto-grants-1981_08 |