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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982360Generated: October 30, 2026

Potassium Iodide → 1-(2-(2-Imidazo[1,2-a]pyridyl)ethyl]-4-(4-methylsulfonylaminobenzoyl)piperidine

https://huagongshe.com/reaction/982360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[4-(piperidine-4-carbonyl)-phenyl]methanesulfonamide hydrochlorideHCID 14130042—
Reactant2-(2-Chloroethyl)imidazo[1,2-a]pyridine hydrochlorideHCID 19801785—
SolventDimethylformamideHCID 6228—
Product1-(2-(2-Imidazo[1,2-a]pyridyl)ethyl]-4-(4-methylsulfonylaminobenzoyl)piperidineHCID 1413005126.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.02 g (3.2 mmol) of 4-(4-methylsulfonylaminobenzoyl)piperidine hydrochloride, 1.34 g of sodium hydrogencarbonate and 10 ml of dimethylformamide was stirred at 80° C. for 1 h. 0.48 g of 2-(2-chloroethyl)imidazo[1,2-a]pyridine hydrochloride and 0.53 g of potassium iodide were added thereto and the mixture was stirred at 80° C. for 2 h. The mixture was filtered and the filtrate was concentrated to obtain a solid residue, which was then purified according to silica gel column chromatography (chloroform:methanol:aqueous ammonia=190:9:1). The fraction of the intended compound was concentrated to obtain a solid residue, which was then recrystallized from ethyl acetate to obtain 0.25 g (yield: 18%) of the intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996215
Source datasetuspto-grants-1991_02
ORD IDord-892c10a484b44b9ca0df392f8ebd7b0c
Source noteuspto-grants-1991_02