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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160988Generated: October 26, 2026

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

https://huagongshe.com/reaction/1160988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl (3-aminopropyl)carbamateHCID 2735700—
Reactant3-fluoro-N,N-bis(3-methylbutyl)-4-nitrobenzamideHCID 68447111—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamateHCID 6878996696%

Reaction Steps

A mixture of 3-fluoro-N,N-bis(3-methylbutyl)-4-nitrobenzamide (1.6 g, 1 eq), N-Boc-1,3-diaminopropane (0.9 g, 1.2 eq) and potassium carbonate (1.35 g, 2 eq) in acetonitrile (80 ml) is heated under reflux for 5 hours then concentrated under reduced pressure at 40° C. The residue is taken up in dichloromethane (100 ml) and water (40 ml). After decantation and extractions, the combined organic phases are washed with salt water, dried over Na2SO4 then concentrated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent: heptane/ethyl acetate 8:2 to 6:4) produces the expected compound in the form of a yellow oil (2.2 g; 96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816539B2
Source datasetuspto-grants-2010_10
ORD IDord-8d2c7bab91d84e57849269d99a3dbc27
Source noteuspto-grants-2010_10