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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429822Generated: October 30, 2026

N-[2-(4-methoxyphenyl)-1-methylethyl]-N-ethyl-[1-(benzyloxycarbonyl)piperidin-4-ylcarbonyl]amine → N-[2-(4-methoxyphenyl)-1-methylethyl]-N-ethyl-(piperidin-4-ylcarbonyl)amine

https://huagongshe.com/reaction/429822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(4-methoxyphenyl)-1-methylethyl]-N-ethyl-[1-(benzyloxycarbonyl)piperidin-4-ylcarbonyl]amineHCID 18352914—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-[2-(4-methoxyphenyl)-1-methylethyl]-N-ethyl-(piperidin-4-ylcarbonyl)amineHCID 1835300484%

Reaction Steps

A mixture of N-[2-(4-methoxyphenyl)-1-methylethyl]-N-ethyl-[1-(benzyloxycarbonyl)piperidin-4-ylcarbonyl]amine (3.5 grams, 8.3 mmole) and 10% palladium on carbon (0.7 grams) in ethanol (40 ml) was hydrogenated at 22° C. and 50 p.s.i. for 2.5 hours. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to leave N-[2-(4-methoxyphenyl)-1-methylethyl]-N-ethyl-(piperidin-4-ylcarbonyl)amine as a syrup (2.11 grams, 84%), M+H 305.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319920B1
Source datasetuspto-grants-2001_11
ORD IDord-e69fbdab26dc4199b1dd630b936c326e
Source noteuspto-grants-2001_11