HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186193Generated: October 31, 2026
4-Iodobenzenesulfonyl chloride → HCID 17798575, compound
https://huagongshe.com/reaction/2186193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Iodobenzenesulfonyl chloride | HCID 7399 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10858694 | HCID 10858694 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 17798575 | HCID 17798575 | 14.3% |
Reaction Steps
To a mixture of 1-[1-(4-pyridyl)-4-piperidylmethyl]-2-piperazinone (549 mg), sodium bicarbonate solution (5 ml), ethyl acetate (10 ml) and THF (5 ml) was added dropwise, under ice-cooling, a solution of 4-iodobenzenesulfonyl chloride (1.21 g) in THF (10 ml), and the mixture was stirred at 0° C. for 1 hour. The separated organic layer was washed with saturated brine, dried (MgSO4) andconcentrated, and the residuewas purifiedwith silica gel column chromatography (acetone:methanol=9:1→1:1) and washed with water to give colorless crystals of 4-(4-iodobenzenesulfonyl)-1-[1-(4-pyridyl)-4-piperidylmethyl]-2-piperazinone (155 mg). A part of the crystals were treated with hydrochloric acid to give colorless crystals of the title compound as hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403595B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-3d0ae7f3596a43d1a716585f59fc7905 |
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| Source note | uspto-grants-2002_06 |
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