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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345448Generated: October 29, 2026

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

https://huagongshe.com/reaction/345448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-([1-(Benzyloxycarbonyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamideHCID 19992429—
SolventEthanolHCID 702—
ProductN-[4-([Piperidin-4-yl]methoxy)phenyl]methanesulphonamideHCID 19992428—

Reaction Steps

A solution of the product of part (iv) (0.15 g) in ethanol was hydrogenated at 50° and 3.5 bar in the presence of 5% palladium on carbon until the required amount of hydrogen had been absorbed. The catalyst was filtered off and washed several times with hot ethanol. The combined filtrate and washings were evaporated to give the product, (0.10 g), m.p. 180°-183°, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057528
Source datasetuspto-grants-1991_10
ORD IDord-d1fb43a210fb4816950c0975a54ae9ff
Source noteuspto-grants-1991_10