Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831480Generated: November 1, 2026

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

https://huagongshe.com/reaction/1831480

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 numberUS07067660B2
Source datasetuspto-grants-2006_06
ORD IDord-80852906d875421e815830747266faf0
Source noteuspto-grants-2006_06