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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382988Generated: October 31, 2026

Methanesulfonyl chloride → HCID 18361514, compound

https://huagongshe.com/reaction/382988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 18361536HCID 18361536—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 18361514HCID 18361514—

Reaction Steps

To a solution of 7-(4-biphenylyl)methoxy-3-[2-(N,N-dimethylamino)ethyl]-1,2,3,4-tetrahydroquinoline (110 mg) in pyridine (5 ml) was added methanesulfonyl chloride (0.03 ml) in an ice bath. The reaction mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried, and concentrated. The residue was purified by alumina column chromatography (eluent: ethyl acetate:hexane=1:2) and converted into its hydrochloride, which was then recrystallized from ethanol-ethyl acetate to obtain the titled compound (88 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310107B1
Source datasetuspto-grants-2001_10
ORD IDord-9240c08f608a45649c4f99737110a0ef
Source noteuspto-grants-2001_10