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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482579Generated: October 30, 2026

Potassium Iodide → 1-(4-(4-(2-furyl)piperazine-1-yl)butyl)-1H-benzimidazole

https://huagongshe.com/reaction/1482579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzimidazole, 1-(4-chlorobutyl)-HCID 583170—
Reactant1-(Furan-2-yl)piperazineHCID 19763577—
SolventAcetonitrileHCID 6342—
Product1-(4-(4-(2-furyl)piperazine-1-yl)butyl)-1H-benzimidazoleHCID 7628242761.6%

Reaction Steps

1-(4-chlorobutyl)-1H-benzimidazole (7.51 g, 0.036 mol) was dissolved into 100 ml of acetonitrile, 4-(2-furyl) piperazine (4.6 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 6.0 g compound (I-12) with a yield of 61.5%. ESI-MS [M+H]+: m/z 325.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09415047B2
Source datasetuspto-grants-2016_08
ORD IDord-d1bfa7a6943341a39f6908f1c9251323
Source noteuspto-grants-2016_08