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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260513Generated: October 26, 2026

N-{3-[4-(5-Benzyloxypyridin-2-yloxy)phenyl]-1-methylpropyl}acetamide → N-{3-[4-(5-Hydroxypyridin-2-yloxy)phenyl]-1-methylpropyl}acetamide

https://huagongshe.com/reaction/1260513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-{3-[4-(5-Benzyloxypyridin-2-yloxy)phenyl]-1-methylpropyl}acetamideHCID 44608622—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-{3-[4-(5-Hydroxypyridin-2-yloxy)phenyl]-1-methylpropyl}acetamideHCID 67302795—

Reaction Steps

N-{3-[4-(5-Benzyloxypyridin-2-yloxy)phenyl]-1-methylpropyl}acetamide (344 mg, 881 μmol) were dissolved in 20 ml of ethanol. Addition of 93 mg of palladium/carbon was followed by hydrogenation under a pressure of 5 bar of hydrogen at room temperature for 16 h. The catalyst was filtered off and the filtrate was concentrated. Yield: 220 mg (83%), M+H+: 301.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470841B2
Source datasetuspto-grants-2013_06
ORD IDord-a2112695a10d44f2bdbf698426baa665
Source noteuspto-grants-2013_06