HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49406Generated: October 29, 2026
Water → N-(3,4-dichloro-5-isothiazolecarbonyl)-N-(4-chlorophenyl)-4-methoxybenzenesulfonamide
https://huagongshe.com/reaction/49406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-(4-Chlorophenyl)-4-methoxybenzenesulfonamide | HCID 598671 | — |
| Reactant | 3,4-Dichloro-5-isothiazolecarbonyl chloride | HCID 10976886 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3,4-dichloro-5-isothiazolecarbonyl)-N-(4-chlorophenyl)-4-methoxybenzenesulfonamide | HCID 11408949 | 36.7% |
Reaction Steps
To a solution of N-(4-chlorophenyl)-4-methoxybenzenesulfonamide (1.98 g) in unhydrous N,N-dimethylformamide (20 ml) 60% sodium hydride (0.24 g) was added at room temperature. After stirring the reaction mixture at the same temperature for 1 hour, a solution of 3,4-dichloro-5-isothiazolecarbonyl chloride (1.1 g) in unhydrous N,N-dimethylformamide (10 ml) was added thereto dropwise. After finishing the addition, the reaction mixture was stirred at room temperature for 18 hours and poured into water. The mixture was extracted with ethyl acetate and the organic phase was washed with water and dried with unhydrous sodium sulfate. The crude product obtained by distilling off the solvent under reduced pressure was recrystallized from ethanol to obtain N-(3,4-dichloro-5-isothiazolecarbonyl)-N-(4-chlorophenyl)-4-methoxybenzenesulfonamide (0.89 g). mp 154-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706748B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-3585ca59184a4e89bbba02979f2ff0d0 |
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| Source note | uspto-grants-2004_03 |
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