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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358444Generated: October 26, 2026

N,N-bis(3-methylbutyl)-4-nitro-3-[(3-piperidin-1-ylpropyl)amino]benzamide → 4-amino-N,N-bis(3-methylbutyl)-3-[(3-piperidin-1-ylpropyl)amino]benzamide

https://huagongshe.com/reaction/2358444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-bis(3-methylbutyl)-4-nitro-3-[(3-piperidin-1-ylpropyl)amino]benzamideHCID 68446148—
CatalystPalladiumHCID 23938—
SolventEthanol ethylacetateHCID 21584252—
Product4-amino-N,N-bis(3-methylbutyl)-3-[(3-piperidin-1-ylpropyl)amino]benzamideHCID 68446348—

Reaction Conditions

Temperature20 °C

Reaction Steps

N,N-bis(3-methylbutyl)-4-nitro-3-[(3-piperidin-1-ylpropyl)amino]benzamide (1 g) in solution in a mixture of ethyl acetate/ethanol 2:1 (100 ml) and 10% palladium on charcoal (100 mg) are introduced into an autoclave. After stirring for 3 hours under a hydrogen atmosphere (3 bars) at a temperature of approximately 20° C., the catalyst is eliminated by filtration on celite and the filtrate is concentrated under reduced pressure at 40° C. in order to produce the expected compound in the form of an oil (910 mg, 97% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763725B2
Source datasetuspto-grants-2010_07
ORD IDord-7916b17770af4521801953241dd59bd9
Source noteuspto-grants-2010_07