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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383094Generated: October 29, 2026

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

https://huagongshe.com/reaction/2383094

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 numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-413d18c9e20447f2b8d242edee652e6c
Source noteuspto-grants-2012_09