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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482605Generated: November 3, 2026

1-(1-Naphthyl)piperazine → 1-(4-(4-(1-naphthyl)piperazine-1-yl)butyl)-1H-benzotriazole

https://huagongshe.com/reaction/1482605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Naphthyl)piperazineHCID 1342—
ReactantPotassium IodideHCID 4875—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-chlorobutyl)-1H-benzotriazoleHCID 3425107—
SolventAcetonitrileHCID 6342—
Product1-(4-(4-(1-naphthyl)piperazine-1-yl)butyl)-1H-benzotriazoleHCID 7628364060.1%

Reaction Steps

1-(4-chlorobutyl)-1H-benzotriazole (7.55 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 and mixed, 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 and purified, eluted with dichloromethane to produce 6.9 g compound (I-47) with a yield of 60.1%. 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-7932926a5b114f10aea020faaee21050
Source noteuspto-grants-2016_08