HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 5-Bromo-N-(2-hydroxyethyl)-3-pyridinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Bromopyridine-3-sulfonyl chloride--hydrogen chloride (1/1) | HCID 44119336 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-N-(2-hydroxyethyl)-3-pyridinesulfonamide | HCID 61795523 | — |
Reaction Steps
A cooled (0° C.) solution of 5-bromopyridine-3-sulfonyl chloride hydrochloride (3.00 g, 10.2 mmol) in DCM (50 ml) was slowly treated with triethylamine (4.3 ml) and stirred until a clear solution was obtained. This solution was treated dropwise with 2-hydroxyethylamine (0.68 g, 0.68 mL) and stirred at RT for 16 hours. The reaction mixture was washed successively with water and brine, the organic layer was dried with sodium sulfate and evaporated under reduced pressure. The crude product was purified by column chromatography (silica) eluting with 20% ethyl acetate in petroleum ether, to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273769B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-d6f78e09dae6452aa0b38b7d0d7b938f |
| Source note | uspto-grants-2012_09 |