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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297640Generated: October 30, 2026

Piperazine → HCID 5255691, compound

https://huagongshe.com/reaction/2297640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 10778001HCID 10778001—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5255691HCID 5255691—

Reaction Steps

To a mixture of 10.0 g (37.9 mmol) of 8,11-dichloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine and 1.0 mL of Et3N in 200 mL of dry THF at room temperature and under a nitrogen atmosphere was added 33.0 g of piperazine. The mixture was stirred at room temperature for 22.5 hours and then refluxed for 5.5 hours. It was then cooled to room temperature, poured into 250 mL of 5% aqueous NaOH, and extracted with CH2Cl2 (3×). The combined organic portions were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified via flash chromatography (2→5% MeOH saturated with NH4OH in CH2Cl2) to yield the title compound as a glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492381B1
Source datasetuspto-grants-2002_12
ORD IDord-e598d201546f41c6aa2e8555504b7810
Source noteuspto-grants-2002_12