HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazol-4-amine → 2,2,2-trifluoro-N-(thiazol-4-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazol-4-amine | HCID 14009640 | — |
| Reactant | N-(2-bromothiazol-4-yl)-2,2,2-trifluoroacetamide | HCID 20377171 | — |
| Product | 2,2,2-trifluoro-N-(thiazol-4-yl)acetamide | HCID 21449659 | — |
Reaction Steps
The method of preparing 4-aminothiazole comprising reacting 2-bromo-4-trifluoroacetamidothiazole under low pressure catalytic hydrogenation conditions in the presence of a noble metal catalyst to give 4-trifluoroacetamidothiazole then reacting said 4-trifluoroacetamidothiazole with sodium or potassium hydroxide in an aqueous medium at from about 30°-35°C. for about 4-8 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03939172 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-1b97e08cca10462d88ec4b3e0cb5471c |
| Source note | uspto-grants-1976_02 |