HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3,4-difluoro-N-(thiazol-2-yl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 3,4-Difluorobenzene-1-sulfonyl chloride | HCID 2736913 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4-difluoro-N-(thiazol-2-yl)benzenesulfonamide | HCID 53513979 | — |
Reaction Steps
To a slurry of 2-aminothiazole (23.88 g, 0.2384 mol) in methylene chloride (150 mL) and pyridine (38.0 mL, 0.470 mol) was added dropwise a solution of 3,4-difluorobenzenesulphonyl chloride (25.0 g, 0.118 mol) in 10 mL of methylene chloride. After stirring for 48 hours the reaction was diluted with more dichloromethane and extracted with 1N HCl. The organic layer was dried over sodium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography to give 3,4-difluoro-N-(thiazol-2-yl)benzenesulfonamide as a white solid. LCMS Rt=1.24 minutes MS m/z 277 [MH]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541588B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-b825268082ba4067a69655ff911ac4af |
| Source note | uspto-grants-2013_09 |