HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267968Generated: October 30, 2026
Ethanesulfonyl chloride → HCID 9910756, compound
https://huagongshe.com/reaction/1267968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | HCID 9885020 | HCID 9885020 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9910756 | HCID 9910756 | 38.4% |
Reaction Steps
2-(3-Chlorophenoxy)-3-[3-(3-aminopyridin-4-yl)propoxy]pyridine (0.15 g, 0.42 mmol) obtained in Example 25 is dissolved in methylene chloride (5 ml) and pyridine (0.34 ml), and thereto is added ethylsulfonyl chloride (0.04 ml, 0.50 mmol) under ice-cooling, and the mixture is stirred for 3 hours. To the mixture is added ice-water (20 ml), and the mixture is extracted with ethyl acetate (50 ml×2). The organic layer is washed with a saturated aqueous sodium hydrogen carbonate solution (20 ml×2) and a saturated brine (20 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by basic silica gel column chromatography (eluent: chloroform/methanol), and further recrystallized from diethyl ether to give the title compound (0.07 g) as colorless crystals, m.p. 131-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06555557B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-39042bda0694406db5c532d02eb967f8 |
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| Source note | uspto-grants-2003_04 |
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