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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598268Generated: October 30, 2026

Ammonium formate → 1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-ol

https://huagongshe.com/reaction/598268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant7-benzyloxy-1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolineHCID 67050917—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-olHCID 13634053656.3%

Reaction Steps

7-Benzyloxy-1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinoline (60.3 g, 0.188 mol), prepared as described in Parts A-G of Example 1, and 10% palladium on carbon (10 g) were mixed with ethanol (500 mL). Ammonium formate (101.53 g, 1.61 mol) and ethanol (500 mL) were then added, and the reaction mixture was heated at reflux for two hours. The mixture was allowed to cool to ambient temperature slowly and stirred overnight. The reaction mixture was filtered through a layer of CELITE filter aid, and the filter cake was washed with ethanol (1 L), methanol (2 L) and dichloromethane (2 L). The combined filtrates were concentrated under reduced pressure to provide a tan solid, which was triturated with cold ethanol and isolated by filtration to yield 30 g of 1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-ol as a tan, granular solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-38621185cd3140eb8be5b4fdb26b2cd4
Source noteuspto-grants-2011_03