HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 6-chloro-N-(1,3-thiazol-2-yl)pyridine-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 2-Chloro-5-pyridinesulfonyl chloride | HCID 2792792 | — |
| Product | 6-chloro-N-(1,3-thiazol-2-yl)pyridine-3-sulfonamide | HCID 943191 | — |
Reaction Steps
To 2-AMINOTHIAZOLE (1.80 g, 0.0179 mol) in Pyridine (6 mL, 0.08 mol) at 0° C. was added 2-Chloropyridine-5-sulfonyl chloride (1.55 g, 0.00717 mol) portion-wise. The reaction mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, diluted with ethyl acetate (150 mL), washed with water and brine. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified on ISCO companion (silica gel, 10% to 100% ethyl acetate in hexanes) to give product as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124610B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-51ae072adf82447784a6626399167d5d |
| Source note | uspto-grants-2012_02 |