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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345447Generated: October 30, 2026

Methanesulfonyl chloride → N-[4-([1-(Benzyloxycarbonyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide

https://huagongshe.com/reaction/345447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-[(4-Aminophenoxy)methyl]-1-(benzyloxycarbonyl)piperidineHCID 19992432—
SolventPyridineHCID 1049—
ProductN-[4-([1-(Benzyloxycarbonyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamideHCID 1999242981.7%

Reaction Steps

Methanesulphonyl chloride (1.91 g) was added to a stirred solution of the product of part (iii) (5.15 g) in pyridine (50 ml) at 0°. The solution was stirred at room temperature for 18 hours and then evaporated. The residue was treated with aqueous sodium bicarbonate solution and the mixture was extracted several times with ethyl acetate. The combined extracts were washed with water, dried (Na2SO4) and evaporated. The residue was crystallised from ethyl acetate/hexane to give the title compound, (5.17 g), m.p. 150°-151°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057528
Source datasetuspto-grants-1991_10
ORD IDord-df94d09ffb7743f89e27dbd011e13789
Source noteuspto-grants-1991_10