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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426348Generated: October 30, 2026

Methanesulfonyl chloride → HCID 69673645, compound

https://huagongshe.com/reaction/1426348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 87944944HCID 87944944—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
SolventCopper SulfateHCID 24462—
ProductHCID 69673645HCID 69673645—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl 4-{3-bromo-5-[(E)-(hydroxyimino)methyl]phenoxy}piperidine-1-carboxylate (157 mg, 0.393 mmol) in pyridine (1.2 mL) was added methanesulfonyl chloride (0.12 mL, 1.6 mmol). The reaction mixture was heated at 60° C. for 2 hours. The reaction solution was diluted with ethyl acetate and saturated CuSO4 solution. The organic layer was washed with CuSO4 twice, 1N HCl, brine, dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography on a silica gel column to give the desired product as white solid. LCMS (M+H)+: 381.1, 383.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933085B2
Source datasetuspto-grants-2015_01
ORD IDord-05004a20c05640a1a78ab3130fd03182
Source noteuspto-grants-2015_01