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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180273Generated: October 30, 2026

1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine → HCID 22180892, compound

https://huagongshe.com/reaction/2180273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
CatalystAdams' catalystHCID 345198—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 22180892HCID 2218089274.3%

Reaction Steps

A catalytic amount of platinum (IV) oxide was added to a solution of 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine (2.75 g, 10.8 mmol) in trifluoroacetic acid (150 mL). The reaction mixture was placed under a hydrogen atmosphere at 50 psi (3.44×105 Pa). After 1 week analysis by mass spectroscopy indicated the presence of both starting material and the tetrahydro product. Fresh catalyst was added to the reaction mixture and hydrogenation was continued at 50 psi (3.44×105 Pa). After 2 weeks the reaction mixture was filtered to remove the catalyst. The filtrate was concentrated under vacuum. The residue was dissolved in 1 N hydrochloric acid (120 mL) and the solution was stirred at ambient temperature for 1 hour. The solution was made basic (pH 10) by the addition of 50% sodium hydroxide and then extracted with dichloromethane (5×100 mL). The extracts were combined and concentrated under vacuum to provide 2.08 g of 1-(4-aminobutyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-4-amine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888000B2
Source datasetuspto-grants-2005_05
ORD IDord-b9441ef78de24206882a4f48fdc0941c
Source noteuspto-grants-2005_05