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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355561Generated: October 31, 2026

3-bromo-2-chloro-5-(4-ethylpiperazin-1-ylsulfonyl)pyridine → HCID 22052242, compound

https://huagongshe.com/reaction/1355561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-bromo-2-chloro-5-(4-ethylpiperazin-1-ylsulfonyl)pyridineHCID 1034224—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 22052242HCID 2205224295%

Reaction Steps

A mixture of 3-bromo-2-chloro-5-(4-ethylpiperazin-1-ylsulfonyl)pyridine (Preparation 9; 6.60 g, 17.9 mmol) and sodium ethoxide (6.09 g, 89.55 mmol) in ethanol (100 mL) was heated under reflux for 18 hours, then cooled. The reaction mixture was concentrated under reduced pressure, the residue partitioned between water (100 mL) and ethyl acetate (100 mL), and the layers separated. The aqueous phase was extracted with ethyl acetate (2×100 mL), the combined organic solutions dried (MgSO4) and evaporated under reduced pressure to afford the title compound as a brown solid (6.41 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586439B2
Source datasetuspto-grants-2003_07
ORD IDord-573457d8934d43cfaac7905f5b6006bf
Source noteuspto-grants-2003_07