HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(4-(3-Aminophenyl)thiazol-2-yl)guanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178419570 | HCID 178419570 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-(3-Aminophenyl)thiazol-2-yl)guanidine | HCID 178512611 | 70.3% |
Reaction Steps
A mixture of 47.1 gm of ethyl N-[3-(2-guanidino-4-thiazolyl)-phenyl]-carbamate hydrobromide, 210 ml of ethanol and 210 ml of a 50% potassium hydroxide solution was refluxed for 15 minutes. After cooling, the white precipitate which had formed was filtered off, dissolved in water and carefully acidified with hydrochloric acid. The resulting solution was made alkaline with an excess of sodium hydroxide solution, and the precipitate formed thereby was filtered off, washed with water and dried, yielding 20 gm of the title compound, m.p. 222°-224° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645841 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-b7f18549302e463d91d20e18689afe3c |
| Source note | uspto-grants-1987_02 |