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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784289Generated: November 1, 2026

Tert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamate → Tert-butyl 3-[(2-amino-5-{[bis(3-methylbutyl)amino]carbonyl}phenyl)amino]propylcarbamate

https://huagongshe.com/reaction/1784289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamateHCID 68789966—
CatalystPalladiumHCID 23938—
SolventEthanol ethylacetateHCID 21584252—
ProductTert-butyl 3-[(2-amino-5-{[bis(3-methylbutyl)amino]carbonyl}phenyl)amino]propylcarbamateHCID 6879210089%

Reaction Conditions

Temperature20 °C

Reaction Steps

Tert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamate (1.65 g) in solution in a mixture of ethyl acetate/ethanol 2:1 (130 ml), and 10% palladium on carbon (165 mg) are introduced into an autoclave. After stirring for 3 hours under a hydrogen atmosphere (3 bar) 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 (1.35 g; 89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501525B2
Source datasetuspto-grants-2009_03
ORD IDord-1b53811f221247c1bb159882d41fbb18
Source noteuspto-grants-2009_03