HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiazolamine, 4-(trifluoromethyl)- → Benzamide, 2,6-dichloro-N-(((4-(trifluoromethyl)-2-thiazolyl)amino)carbonyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiazolamine, 4-(trifluoromethyl)- | HCID 1201417 | — |
| Reactant | 2,6-Dichlorobenzoyl isocyanate | HCID 12912739 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzamide, 2,6-dichloro-N-(((4-(trifluoromethyl)-2-thiazolyl)amino)carbonyl)- | HCID 13422728 | — |
Reaction Steps
To a solution of 1.7 g (0.01 mole) of 4-trifluoromethyl-2-aminothiazole in 50 ml of dry ethylacetate was added all at once to a solution of 2.16 g (0.01 mole) of freshly prepared 2,6-dichlorobenzoylisocyanate dissolved in 10 ml of dry ethylacetate. The mixture was allowed to stir at 25° for 4 hours. The solvent was evaporated in vacuo, ether was added to the residue, and the solid was removed by filtration to give 3.7 g of product, m.p. 210°-213°. The infrared and nuclear magnetic resonance spectra were consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04164581 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-be49ba30bdb1483ab7da7314c174ac7e |
| Source note | uspto-grants-1979_08 |