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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390133Generated: October 29, 2026

Ethanolamine → 5-Bromo-N-(2-hydroxyethyl)-3-pyridinesulfonamide

https://huagongshe.com/reaction/2390133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantTriethylamineHCID 8471—
Reactant5-Bromopyridine-3-sulfonyl chloride--hydrogen chloride (1/1)HCID 44119336—
SolventDichloromethaneHCID 6344—
Product5-Bromo-N-(2-hydroxyethyl)-3-pyridinesulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273769B2
Source datasetuspto-grants-2012_09
ORD IDord-d6f78e09dae6452aa0b38b7d0d7b938f
Source noteuspto-grants-2012_09