HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[2-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]acetylamino]benzenesulfonic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfanilic acid | HCID 8479 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]acetic acid | HCID 15676555 | — |
| Reactant | HCID 178526939 | HCID 178526939 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[2-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]acetylamino]benzenesulfonic Acid | HCID 19763995 | — |
Reaction Steps
Under the conditions of Example 2(a), 3.012 g (10 mmol) of 2-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]acetic acid, 1.732 g (10 mmol) of 4-aminobenzenesulfonic acid, 1.531 g (10 mmol) of hydroxybenzotriazole, hydrate, as well as 1.012 g (10 mmol) of triethylamine and 2.063 g (10 mmol) of dicyclohexylcarbodiimide are reacted and worked up analogously. The crude product is dissolved in distilled water, extracted with ethyl acetate, and converted into the free acid by treatment with acidic cation exchanger, thus obtaining the title compound by freeze-drying of the aqueous solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210290 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-b95fea6ea28f428c8f5b2ec8d40e39c2 |
| Source note | uspto-grants-1993_05 |