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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248747Generated: October 30, 2026

Triethylamine → 4-[2-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]acetylamino]benzenesulfonic Acid

https://huagongshe.com/reaction/248747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfanilic acidHCID 8479—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]acetic acidHCID 15676555—
ReactantHCID 178526939HCID 178526939—
SolventWaterHCID 962—
Product4-[2-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]acetylamino]benzenesulfonic AcidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210290
Source datasetuspto-grants-1993_05
ORD IDord-b95fea6ea28f428c8f5b2ec8d40e39c2
Source noteuspto-grants-1993_05