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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603587Generated: October 31, 2026

Piperazine → HCID 10982183, compound

https://huagongshe.com/reaction/1603587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
Reactant4-[(2,6-Dibromo-4-pyridinyl)sulfonyl]anilineHCID 11014674—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10982183HCID 1098218382.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

0.275 g (0.0007 mol) of 4-(2,6-dibromopyridine-4-sulphonyl)-phenylamine was dissolved in 10 ml of dioxane and treated with 0.066 g (0.00077 mol) of piperazine and 1 ml of triethylamine. The mixture was stirred at 40° C. for 72 hrs. and the solvent was then removed. The residue was partitioned in ethyl acetate and water and the organic phase was extracted with sat. sodium chloride solution and dried over MgSO4 and filtered. After removal of the solvent the residue was chromatographed on silica gel with dichloromethane/methanol 9:1 and there was obtained 0.23 g (82%) of 4-(2-bromo-6-piperazin-1-ylpyridin-4-sulphonyl) -phenylamine as yellowish crystals; m.p.: 173-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-1f8bb73f991f4c5bb070ff7f5bddebe2
Source noteuspto-grants-1999_11