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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982358Generated: October 25, 2026

Potassium Iodide → 4-(4-Methylsulfonylaminobenzoyl)-1-[2-(3-pyridyl)ethyl]piperidine dihydrochloride

https://huagongshe.com/reaction/982358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantPyridine, 3-(2-chloroethyl)-, hydrochlorideHCID 199465—
ReactantN-[4-(piperidine-4-carbonyl)-phenyl]methanesulfonamide hydrochlorideHCID 14130042—
SolventDimethylformamideHCID 6228—
Product4-(4-Methylsulfonylaminobenzoyl)-1-[2-(3-pyridyl)ethyl]piperidine dihydrochlorideHCID 1413004628.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

35 g (0.101 mol) of 4-(4-methylsulfonylaminobenzoyl)piperidine hydrochloride and 55 g of potassium carbonate were suspended in 700 ml of dimethylformamide and the suspension was stirred at 40° C. for 20 min. 19.6 g (0.101 mol) of 3-(2-chloroethyl)pyridine hydrochloride and 6.0 g (0.036 mol) of potassium iodide were added to the suspension and the mixture was stirred at 90° C. for 3.5 h. The liquid reaction mixture was filtered and the filtrate was concentrated, while the residue was purified according to silica gel chromatography (chloroform:methanol=93:7). The purified product was converted into its hydrochloride with ethanolic hydrogen chloride and recrystallized from methanol/isopropanol to obtain 13.4 g of the intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996215
Source datasetuspto-grants-1991_02
ORD IDord-45fa37e1bbff4bbba6c3b088319bb08f
Source noteuspto-grants-1991_02