HuagongsheHuagongshe Chemistry Print Report · For research reference only
Taurine → 2-[2-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]acetylamino]ethanesulfonic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Taurine | HCID 1123 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| 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 | 2-[2-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]acetylamino]ethanesulfonic Acid | HCID 19764022 | — |
Reaction Steps
Under the conditions of Example 2(a), 3.012 g (10 mmol) of 2-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]acetic acid, 1.252 g (10 mmol) of 2aminoethanesulfonic 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. The title compound is obtained by freeze-drying the aqueous solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210290 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-2d8c875dee1d4a2eaae5ac95928e4f7c |
| Source note | uspto-grants-1993_05 |