HuagongsheHuagongshe Chemistry Print Report · For research reference only
Felbinac → N-methyl-N-(4-methyl-5-sulfamoyl-thiazol-2-yl)-2-(4-phenylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Felbinac | HCID 3332 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 4-Methyl-2-(methylamino)-1,3-thiazole-5-sulfonamide | HCID 11275781 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-methyl-N-(4-methyl-5-sulfamoyl-thiazol-2-yl)-2-(4-phenylphenyl)acetamide | HCID 5278580 | — |
Reaction Steps
138.2 mg (0.65 mmol) of 4-biphenylacetic acid and 99.7 mg (0.65 mmol) of 1-hydroxy-1H-benzotriazole hydrate are initially charged at room temperature in 5 ml of dimethylformamide. 150 mg (0.72 mmol) of 2-methylamino-4-methyl-1,3-thiazole-5-sulphonamide and 138.7 mg (0.72 mmol) of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride are added, and the mixture is stirred at room temperature for 72 h. The reaction mixture is then filtered off with suction and the residue is recrystallized from 2-propanol. This gives a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105553B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-96aa32fd65a2407f8fdea9239f621c0e |
| Source note | uspto-grants-2006_09 |