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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354260Generated: November 3, 2026

Diisopropylethylamine → 1-[2-(5-Fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine

https://huagongshe.com/reaction/1354260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-fluoro-1H-benzimidazole-2-thiolHCID 3434885—
Reactant4-(2-Hydroxyethyl)piperazine-1-carbaldehydeHCID 9942213—
Reactant(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
SolventWaterHCID 962—
SolventPropionitrileHCID 7854—
Product1-[2-(5-Fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazineHCID 2311615880%

Reaction Conditions

Temperature92 °C

Reaction Steps

1-Formyl-4-(2-hydroxyethyl)piperazine (1.20 g, 7.6 mmol), 5-fluoro-2-mercaptobenzimidazole (1.28 g, 7.6 mmol), and diisopropylethylamine (3.93 g, 30.4 mmol) was dissolved in propionitrile (50 mL), and cyanomethyltrimethylphosphonium iodide (7.39 g, 30.4 mmol) was added to the mixture, followed by stirring for one hour at 92° C. under argon. The reaction mixture was allowed to cool and then poured into water (100 mL), followed by extraction with chloroform (100 mL×3) The resultant organic layer was washed with saturated brine and then dried over sodium sulfate anhydrate, followed by concentration under reduced pressure. The crude product was crystallized from acetone-ether, to thereby yield 1-[2-(5-fluorobenzimidazol-2-ylthio)ethyl]-4-formylpiperazine (1.87 g, yield 80%) as a brown crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223764B2
Source datasetuspto-grants-2007_05
ORD IDord-27a4d1b7b6ce4a5a8e5779686c918492
Source noteuspto-grants-2007_05