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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9452Generated: October 25, 2026

(7-Bromo-3-nitroquinolin-4-yl)isobutylamine → 7-bromo-N4-isobutylquinoline-3,4-diamine

https://huagongshe.com/reaction/9452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(7-Bromo-3-nitroquinolin-4-yl)isobutylamineHCID 21984282—
CatalystPlatinumHCID 23939—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
Product7-bromo-N4-isobutylquinoline-3,4-diamineHCID 68818159—

Reaction Steps

A solution of (7-bromo-3-nitroquinolin-4-yl)-(2-methylpropyl)amine (30.9 g, 105 mmol) in acetonitrile (1.8 L) and isopropanol (200 mL) was added to a Parr vessel. A mixture of 5% platinum on carbon (3.0 g) and acetonitrile:isopropanol (20 mL) was added, and the vessel was purged with nitrogen. The vessel was placed under hydrogen pressure (40 psi, 2.8×105 Pa) for two hours. After one hour, the pressure had decreased to 20 psi (1.4×105 Pa) and was readjusted to 40 psi (2.8×105 Pa). The reaction mixture was filtered through a layer of CELITE filter aid, and the filter cake was washed with acetonitrile. The filtrate was concentrated under reduced pressure to provide 7-bromo-N4-(2-methylpropyl)quinoline-3,4-diamine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091214B2
Source datasetuspto-grants-2006_08
ORD IDord-aae0dad34e834b03a63c256ec63dadca
Source noteuspto-grants-2006_08