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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482583Generated: October 31, 2026

1-(1-Naphthyl)piperazine → HCID 76282429, compound

https://huagongshe.com/reaction/1482583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Naphthyl)piperazineHCID 1342—
ReactantPotassium IodideHCID 4875—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzimidazole, 1-(4-chlorobutyl)-HCID 583170—
SolventAcetonitrileHCID 6342—
ProductHCID 76282429HCID 7628242959.1%

Reaction Steps

1-(4-chlorobutyl)-1H-benzimidazole (7.51 g, 0.036 mol) was dissolved into 100 ml of acetonitrile, 4-(1-naphthyl) piperazine (6.4 g, 0.03 mol), diisopropylethylamine (15.5 g, 0.12 mol) and potassium iodide (5.0 g, 0.03 mol) were respectively added. The mixture was stirred for 10 min at ambient temperature, and then heated and refluxed to react for 20 hours. The mixture was cooled down to ambient temperature and filtered. The filtrate was concentrated to produce oily products, and treated by chromatography with neutral Al2O3, eluted with dichloromethane/methanol mixture to produce 6.8 g compound (I-16) with a yield of 59.1%. ESI-MS [M+H]+: m/z 385.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09415047B2
Source datasetuspto-grants-2016_08
ORD IDord-93696e25fa25494382d9576b247798a2
Source noteuspto-grants-2016_08