HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087222Generated: November 1, 2026
Potassium Hydroxide → N-ethyl-3-(2,4-difluorophenylthio)-4-(methanesulfonamido)benzamide
https://huagongshe.com/reaction/1087222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-ethyl4-amino-3-(2,4-difluorophenylthio)benzamide | HCID 10086583 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-ethyl-3-(2,4-difluorophenylthio)-4-(methanesulfonamido)benzamide | HCID 10430237 | 63.6% |
Reaction Steps
A mixture of N-ethyl-4-amino-3-(2,4-difluorophenylthio)benzamide (0.84 g) and methanesulfonyl chloride (0.57 g) in pyridine (5 ml) was stirred at room temperature overnight. The reaction mixture was concentrated. The residue was dissolved in ethyl acetate, washed with dilute hydrochloric acid, dried and evaporated. The residue obtained was dissolved in methanol and treated with potassium hydroxide (0.4 g). The solution was concentrated and the residue was dissolved in water. The aqueous solution was acidified with dilute hydrochloric acid and extracted with chloroform. The extract was washed with water, dried, and evaporated. The residual solid was recrystallized from ethanol to give N-ethyl-3-(2,4-difluorophenylthio)-4-(methanesulfonamido)benzamide (0.67 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034417 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-73566f6c54e14f18bc05c20828ae90f6 |
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| Source note | uspto-grants-1991_07 |
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