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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910864Generated: October 31, 2026

Pyridine → HCID 11697421, compound

https://huagongshe.com/reaction/910864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantHCID 67391135HCID 67391135—
SolventDichloromethaneHCID 6344—
ProductHCID 11697421HCID 11697421—

Reaction Steps

Ethanesulphonyl chloride (0.1 ml) was added to a mixture of the product from step (iii) (0.11 g) and pyridine (0.5 ml) in DCM (4 ml). After stirring at room temperature for 4 h the mixture was partitioned between diethylether/2 M HCl. The organics separated, dried and evaporated under reduced pressure. The residue was dissolved in methanol (5 ml) then 2M NaOH added and stirred at room temperature for 20 h. The solvent was removed under reduced pressure and the residue partitioned between ethylacetate/1M HCl. The organics were separated, washed with water, dried and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 80% ethylacetate/isohexane, yield 0.025 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022248B2
Source datasetuspto-grants-2011_09
ORD IDord-8b6f19d406f74165a1654660331abe3a
Source noteuspto-grants-2011_09