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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-[4-(piperidine-4-carbonyl)-phenyl]methanesulfonamide hydrochloride | HCID 14130042 | — |
| Reactant | 2-(2-Chloroethyl)imidazo[1,2-a]pyridine hydrochloride | HCID 19801785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-(2-Imidazo[1,2-a]pyridyl)ethyl]-4-(4-methylsulfonylaminobenzoyl)piperidine | HCID 14130051 | 26.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04996215 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-892c10a484b44b9ca0df392f8ebd7b0c |
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| Source note | uspto-grants-1991_02 |
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