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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72678Generated: October 25, 2026

1-(5-Nitropyridin-2-yl)piperazine → HCID 25004371, compound

https://huagongshe.com/reaction/72678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Nitropyridin-2-yl)piperazineHCID 2928799—
Reactant3-[6-Chloro-5-phenyl-2-(trifluoromethyl)pyrimidin-4-yl]benzenesulfonamideHCID 86613621—
SolventPyridineHCID 1049—
ProductHCID 25004371HCID 25004371—

Reaction Steps

The solution of 3-[6-chloro-5-phenyl-2-(trifluoromethyl)pyrimidin-4-yl]benzenesulfonamide (0.1 g, 0.242 mmol) in pyridine (2 ml) was treated with 1-(5-nitropyridin-2-yl)piperazine (0.075 g, 0.363 mmol) and stirred for 11 hours. Subsequently the reaction mixture was poured onto ice-cold water and extracted with ethyl acetate (25 ml). The organic layer was washed with brine and evaporated to give the crude material. Purification by column chromatography (elution with 70% ethyl acetate in hexane) yielded the title compound. 1H-NMR (CDCl3) δ: 3.45-3.46 (m, 4H), 3.72 (m, 4H), 6.52-6.54 (d, 1H), 7.08-7.11 (d, 2H), 7.21-7.26 (m, 2H), 7.32-7.34 (d, 1H), 7.40-7.42 (d, 1H), 7.50 (m, 1H), 7.68 (s, 1H), 7.84-7.89 (m, 1H), 8.21-8.23 (d, 1H), 8.99 (s, 1H); MS m/z: 585.8 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828999B2
Source datasetuspto-grants-2014_09
ORD IDord-c71cebf072604b6681de1c00a59ebdd7
Source noteuspto-grants-2014_09