HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46314Generated: October 29, 2026
Hydrochloric Acid → N-(5-chloro-1,3-thiazol-2-yl)-3-cyano-4-(4-fluoro-2-iodophenoxy)benzenesulfonamide
https://huagongshe.com/reaction/46314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-2-iodophenol | HCID 10171417 | — |
| Reactant | N-(5-chloro-thiazol-2-yl)-3-cyano-4-fluorobenzenesulfonamide | HCID 59436522 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5-chloro-1,3-thiazol-2-yl)-3-cyano-4-(4-fluoro-2-iodophenoxy)benzenesulfonamide | HCID 59436633 | 59% |
Reaction Steps
To a solution of N-(5-Chloro-1,3-thiazol-2-yl)-3-cyano-4-fluorobenzenesulfonamide (Preparation 52, 100 mg, 0.32 mmol) and potassium carbonate (109 mg, 0.8 mmol) in dimethylformamide (3 ml) was added 4-fluoro-2-iodophenol (Preparation 218, 0.32 mmol) and the reaction heated at 80° C. for 24 hours. The solution was added dropwise into rapidly stirring hydrochloric acid (2M aqueous solution). The fine dark precipitate was filtered and dried in vacuo to afford the title product as a brown solid, 100 mg, 59% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541588B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-69f75e533d9a46c688a2f550dc3510e0 |
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| Source note | uspto-grants-2013_09 |
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