HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-bromo-N-(thiazol-2-yl)pyridine-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 5-Bromopyridine-2-sulfonyl chloride | HCID 44558097 | — |
| Product | 5-bromo-N-(thiazol-2-yl)pyridine-2-sulfonamide | HCID 57551252 | — |
Reaction Steps
To 2-AMINOTHIAZOLE (0.29 g, 0.0029 mol) in Pyridine (2 mL, 0.02 mol) was added portionwise 5-Bromo-pyridine-2-sulfonyl chloride (0.50 g, 0.0019 mol). The reaction mixture was stirred at room temperature for 24 h. The reaction mixture was concentrated under reduced pressure, diluted with Ethyl acetate, washed with 1.0 N HCl, H2O and brine, dried with anhydrous sodium sulfate, filtered and concentrated to give the product was obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124610B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-732c5ad9834d4e549b77dc9f1449d92f |
| Source note | uspto-grants-2012_02 |