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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355153Generated: October 31, 2026

Diisopropylethylamine → (5S)-5-({[4-(4-fluorophenyl)piperidin-1-yl}sulfonyl]methyl)-5-methylimidazolidine-2,4-dione

https://huagongshe.com/reaction/2355153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(4S)-(4-methyl-2,5-dioxoimidazolidin-4-yl)methanesulphonyl chlorideHCID 16738713—
Reactant4-(4-Fluoro-phenyl)-piperidine hydrochlorideHCID 21898168—
SolventTetrahydrofuranHCID 8028—
Product(5S)-5-({[4-(4-fluorophenyl)piperidin-1-yl}sulfonyl]methyl)-5-methylimidazolidine-2,4-dioneHCID 59794371—

Reaction Conditions

Temperature50 °C

Reaction Steps

4-(4-Fluorophenyl)piperidine hydrochloride (63 mg, 0.29 mmol) was taken up in 3 mL of dry THF, neutralized with diisopropylethylamine (50 μL, 0.29 mmol) and cooled on an ice-water bath. [(4S)-4-methyl-2,5-dioxo-imidazolodin-4-yl]methanesulfonyl chloride (80 mg, 0.35 mmol) was added and after stirring for 10 min, diisopropylethylamine (50 μL, 0.29 mmol) was added and the reaction mixture was stirred at ambient temperature until LC-MS (APCI) indicated consumption of the amine. The reaction mixture was evaporated and the residue taken up in EtOH and heated to 50° C. and allowed to cool before water was added. The precipitated product was collected and washed with EtOH/water and dried in vacuum to yield 87 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754750B2
Source datasetuspto-grants-2010_07
ORD IDord-d7eca5ecbe404b4c8add264ee9f843cd
Source noteuspto-grants-2010_07