HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-Bromo-2-fluoro-N-thiazol-2-yl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Bromo-2-fluorobenzene-1-sulfonyl chloride | HCID 2736310 | — |
| Product | 4-Bromo-2-fluoro-N-thiazol-2-yl-benzenesulfonamide | HCID 25138353 | 36% |
Reaction Steps
To a solution of 2-aminothiazole (4.51 g, 0.0450 mol) and pyridine (24.26 mL, 0.3000 mol) in methylene chloride (40 mL, 0.6 mol) at 0° C. was added portionwise 4-bromo-2-fluorobenzenesulfonyl chloride (8.2 g, 0.030 mol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, diluted with EtOAc, washed with 1N HCl solution, H2O and brine. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated to give the crude product that was purified via automated flash chromatography (silica gel, 25% EtOAc in hexanes to 100% EtOAc) to give the product as a light brown solid (3.6 g, 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124610B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-a7de876b12d84a268667377c93faf3d1 |
| Source note | uspto-grants-2012_02 |