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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784288Generated: November 1, 2026

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

https://huagongshe.com/reaction/1784288

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 numberUS07501525B2
Source datasetuspto-grants-2009_03
ORD IDord-38eb5f54a0d64a3aa3aa1ffb2c8dfec8
Source noteuspto-grants-2009_03