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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910819Generated: November 2, 2026

1-(4-Nitrophenyl)piperazine → HCID 67106340, compound

https://huagongshe.com/reaction/1910819

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
ReactantPyridine-3-sulfonyl chlorideHCID 3164136—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67106340HCID 6710634039%

Reaction Steps

To a solution of 1-(4-nitrophenyl)-piperazine (2.50 g, 12.1 mmol) in pyridine (15 mL) was added a solution of pyridine-3-sulfonyl chloride (2.78 g, 15.7 mmol) in THF (30 mL) under an argon atmosphere at 0° C. The reaction was warmed to r.t. and stirred for 2 h, before the mixture was evaporated to dryness. The residue was partitioned between water and dichloromethane, the organic layer separated and washed successively with sat. sodium bicarbonate solution, water and brine. The organics were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was subjected to column chromatography over neutral alumina using 5% to 70% ethyl acetate in petroleum ether as eluent to afford 1-(4-nitrophenyl)-4-(pyridine-3-sulfonyl)-piperazine (1.63 g, 39%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604029B2
Source datasetuspto-grants-2013_12
ORD IDord-b3cf5a73760c4cbdaaaf5e2246f9cfb4
Source noteuspto-grants-2013_12