HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591016Generated: November 1, 2026
Sulfanilamide → 4-(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propanamido)benzenesulfonamide
https://huagongshe.com/reaction/1591016
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxypropionic acid chloride hydrochloride | HCID 88451402 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propanamido)benzenesulfonamide | HCID 14498554 | 80.8% |
Reaction Steps
(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propionic acid chloride hydrochloride (0.8 g) and 4-aminobenzene sulfonamide (0.5 g) were dissolved in dry tetrahydrofuran (20 ml), and the solution was stirred, with an addition of triethylamine (0.6 ml) at room temperature for 2 hours. After completion of the reaction, the solvent was evaporated under a reduced pressure, the residue was dissolved in methylene chloride and washed with 1 N hydrochloric acid, water, saturated aqueous sodium hydrogen carbonate, water and saturated aqueous sodium chloride After drying over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under a reduced pressure was purified by medium pressure column chromatography by using silica gel, to obtain the title compound (0.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05205855 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-36f182a8739449d2acf0bf3152953ca8 |
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| Source note | uspto-grants-1993_04 |
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