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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203543Generated: October 31, 2026

3-Furanol, tetrahydro- → 1-(2-methylpropyl)-2-propyl-7-(tetrahydrofuran-3-yloxy)-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/2203543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Furanol, tetrahydro-HCID 9960—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-olHCID 136340536—
SolventTetrahydrofuranHCID 8028—
Product1-(2-methylpropyl)-2-propyl-7-(tetrahydrofuran-3-yloxy)-1H-imidazo[4,5-c]quinolineHCID 6897000488.9%

Reaction Steps

3-Hydroxytetrahydrofuran (0.375 mL, 4.64 mmol) was added to a suspension of 1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-ol (1.0 g, 3.5 mmol) and triphenylphosphine (1.5 g, 5.7 mmol) in THF. Diisopropyl azodicarboxylate (1.1 mL, 5.6 mmol) was added dropwise over a period of three minutes, and the reaction was stirred for 48 hours. The solvent was removed under reduced pressure, the residue was purified by column chromatography on silica gel (eluting with 98:2 dichloromethane:methanol) to provide 1.1 g of 1-(2-methylpropyl)-2-propyl-7-(tetrahydrofuran-3-yloxy)-1H-imidazo[4,5-c]quinoline as an off-white, crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365567B2
Source datasetuspto-grants-2016_06
ORD IDord-f592239c12894e4180dcc83f25c38c06
Source noteuspto-grants-2016_06