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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789413Generated: October 30, 2026

Isobutylamine → 4-Isobutylamino-3-nitroquinoline

https://huagongshe.com/reaction/1789413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
SolventTetrahydrofuranHCID 8028—
Product4-Isobutylamino-3-nitroquinolineHCID 10999310—

Reaction Steps

To a stirred solution of 50.Og (0.24 mole) of 4-chloro-3-nitroquinoline in 300 ml of tetrahydrofuran was added, in small portions, 52.7g (0.72 mole) of isobutylamine. The mixture was heated at its reflux temperature for one hour, and was then evaporated in vacuo. Water was added to the residue and the solid was separated by filtration. The solid was suspended in one liter of water, and was dissolved by the gradual addition of concentrated hydrochloric acid (to pH 3 to 4), at which time the solution was filtered. The filtrate was basified (to pH 9 to 10) by the addition of concentrated ammonium hydroxide to provide bright yellow 4-(isobutylamino)-3-nitroquinoline, m.p. 119°-121° C. The structural assignment was supported by infrared spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689338
Source datasetuspto-grants-1987_08
ORD IDord-2a25a670f29446a8bcfed9c8a1b1ea10
Source noteuspto-grants-1987_08