HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110674Generated: November 2, 2026
Sulfanilamide → 4-(2-(4-(3-Chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propanamido)benzenesulfonamide
https://huagongshe.com/reaction/1110674
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 1N 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 | US04976773 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-4dd32cb082864481a5ad96100b6af56c |
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| Source note | uspto-grants-1990_12 |
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