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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345437Generated: October 29, 2026

N-[4-([1-(4-nitro-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide → N-[4-([1-(4-Amino-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide

https://huagongshe.com/reaction/345437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-([1-(4-nitro-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamideHCID 19992415—
SolventEthanolHCID 702—
ProductN-[4-([1-(4-Amino-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamideHCID 1999242792.5%

Reaction Steps

A solution of N-[4-([1-(4-nitro-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide (see Preparation 5) (140 mg) in ethanol (50 ml) was hydrogenated at room temperature 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 the filtrate was evaporated to give the product (120 mg), m.p. 213°-214° (from ethyl acetate/methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057528
Source datasetuspto-grants-1991_10
ORD IDord-fc52c9c135ce4bacbf73adfbb7d451e5
Source noteuspto-grants-1991_10