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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581748Generated: October 30, 2026

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

https://huagongshe.com/reaction/1581748

Reaction equation

Participants

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

Reaction Steps

A mixture of the product from stage d) (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; Found C, 41.27; H, 5.33; N, 11.11. C13H20BrN3O3S requires C, 41.35; H, 5.28; N, 10.99%; δ (CDCl3, 300 MHz) 1.06 (3H, t), 1.48 (3H, t), 2.42 (2H, q), 2.56 (4H, m), 3.09 (4H, m), 4.54 (2H, q), 8.10 (1H, s), 8.46 (1H, s); LRMS: m/z 378, 380 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730786B2
Source datasetuspto-grants-2004_05
ORD IDord-f37cfb90bedc45b28e247cb4c59a4eaf
Source noteuspto-grants-2004_05