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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255516Generated: November 1, 2026

Methylamine → 4-Methylamino-3-nitroquinoline

https://huagongshe.com/reaction/255516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
SolventWaterHCID 962—
Product4-Methylamino-3-nitroquinolineHCID 13958321—

Reaction Steps

To a stirred solution of 40% aqueous methylamine was added, in small portions, 30.0 g (0.144 mole) of 4-chloro-3-nitroquinoline. The reaction mixture was then heated at its reflux temperature for about 0.75 hour. After cooling, the mixture was poured in 300 ml of water. The solid was separated by filtration, and was then suspended in 300 ml of water. Acidification with 6N hydrochloric acid to pH 3 to 4 effected dissolution of most of the solid. Filtration was followed by basification of the filtrate with concentrated ammonium hydroxide to pH 8 to 10 to provide a yellow precipitate. The solid was separated by filtration, washed with water, and recrystallized from ethanol to provide yellow 4-methylamino-3-nitroquinoline, m.p. 168°-170° C. Analysis: Calculated for C10H9N3O2 %C, 59.1; %H, 4.5; %N, 20.7; Found: %C, 59.0; %H, 4.2; %N, 20.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698348
Source datasetuspto-grants-1987_10
ORD IDord-d794f459c09e484fa961ea9d92ad8a4c
Source noteuspto-grants-1987_10