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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746567Generated: October 29, 2026

1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine → HCID 22344444, compound

https://huagongshe.com/reaction/746567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 22180872—
CatalystAdams' catalystHCID 345198—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 22344444HCID 2234444445%

Reaction Steps

A catalytic amount of platinum (IV) oxide was added to a solution of 1-(4-aminobutyl)-2-methoxyethyl-1H-imidazo[4,5-c]quinolin-4-amine (7.7 g, 24.5 mmol) in trifluoroacetic acid (250 mL). The reaction mixture was hydrogenated at 50 psi (3.44×105 Pa) on a Parr apparatus. The progress of the reaction was monitored by LC/MS. Additional catalyst was added 7, 11, and 17 days after the start of the reaction. After 25 days the reaction was complete. The reaction mixture was filtered through a layer of Celite® filter aid to remove the catalyst and the filtrate was concentrated under vacuum. The residue was combined with 1 N hydrochloric acid (100 mL) and stirred overnight. The mixture was made basic (pH=11) with ammonium hydroxide and then extracted with dichloromethane (3×300 mL). The extracts were combined and concentrated under vacuum to provide 3.5 g of 1-(4-aminobutyl)-6,7,8,9-tetrahydro-2-methoxyethyl-1H-imidazo[4,5-c]quinolin4-amine as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393859B2
Source datasetuspto-grants-2008_07
ORD IDord-e68f25643b544e9aa8590b4388ba1a40
Source noteuspto-grants-2008_07