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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097600Generated: October 30, 2026

Ammonia → 1-(2-aminoethyl)-1H-imidazo[4,5-c]quinoline-2,4-diamine

https://huagongshe.com/reaction/1097600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactanttert-butyl 2-(2-amino-4-chloro-1H-imidazo[4,5-c]quinolin-1-yl)ethylcarbamateHCID 86626304—
SolventMethanolHCID 887—
Product1-(2-aminoethyl)-1H-imidazo[4,5-c]quinoline-2,4-diamineHCID 66814500—

Reaction Conditions

Temperature150 °C

Reaction Steps

tert-Butyl 2-(2-amino-4-chloro-1H-imidazo[4,5-c]quinolin-1-yl)ethylcarbamate (3.5 g, 9.7 mmol) and ammonia (approximately 100 mL of a 7 N solution in methanol) were added to a pressure vessel, which was sealed and heated at 150° C. overnight. The volatiles were removed under reduced pressure, and the residue was purified by automated flash chromatography (silica cartridge, eluting with aqueous ammonium hydroxide:methanol:dichloromethane in a gradient from 0:0:100 to 1.5:28.5:70) to provide 840 mg of 1-(2-aminoethyl)-1H-imidazo[4,5-c]quinoline-2,4-diamine as a dark grey solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143270B2
Source datasetuspto-grants-2012_03
ORD IDord-bd7fc6e343e044c1b5e4e539a9456fb4
Source noteuspto-grants-2012_03