HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-(2-Thiazolyl)propylguanidine hemisulphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | S-methyl isothiourea hemisulfate | HCID 6604939 | — |
| Reactant | 3-(1,3-Thiazol-2-yl)propan-1-amine | HCID 11686921 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(2-Thiazolyl)propylguanidine hemisulphate | HCID 178512792 | — |
Reaction Steps
3-(2-Thiazolyl)propylamine (2.7 g) (prepared from the amine dihydrochloride by reaction with aqueous sodium hydroxide and extraction with ethyl acetate) is mixed intimately with finely powdered S-methylthiouronium sulphate (5.3 g) and the mixture is heated at 140°-150°C for 1 hour. After cooling, the mass is extracted with hot ethanol several times, and the combined extracts are diluted with ether which causes the precipitation of a white solid. Recrystallization from aqueous ethanol yields 3-(2-thiazolyl)propylguanidine hemisulphate, m.p. 160°-163°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03968216 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-bc568d28cc0c418687bbec3dd218b2e6 |
| Source note | uspto-grants-1976_07 |