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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603600Generated: November 1, 2026

Piperazine → HCID 19605480, compound

https://huagongshe.com/reaction/1603600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
ReactantHCID 19605520HCID 19605520—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 19605480HCID 1960548062.2%

Reaction Steps

0.222 g (0.0005 mol) of 2,6-dibromo-4-(3-trifluoromethylbenzenesulphonyl)-pyridine was dissolved in 10 ml of dioxan and treated with 0.047 g (0.00055 mol) of piperazine and 0.7 ml of triethylamine. The mixture was stirred at room temperature for 20 hrs. and subsequently at 40° C. for 3 hrs., the solvent was then removed and the residue was chromatographed on silica gel with 5% methanol in dichloromethane. There was obtained 0.14 g (62%) of 1-[6-bromo-4-(3-trifluoromethylbenzenesulphonyl)-pyridin-2-yl]-piperazine as yellow crystals; m.p.: 160-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-e7ee79a48de84c31b35b86ca28bb32ee
Source noteuspto-grants-1999_11