Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598342Generated: October 29, 2026

Pyridine → [7-Benzyloxy-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol

https://huagongshe.com/reaction/598342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Methoxypropanoyl chlorideHCID 2759728—
ReactantHCID 67050960HCID 67050960—
SolventTolueneHCID 1140—
Product[7-Benzyloxy-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-olHCID 6705112975.6%

Reaction Steps

1-(3-Amino-7-benzyloxyquinolin-4-ylamino)-2-methyl-propan-2-ol (25 g, 74.09 mmol) was added to 500 mL of pyridine. To this mixture was added in a dropwise manner a solution of methoxypropionyl chloride (10 g, 81.5 mmol) dissolved in 20 mL of toluene. After approximately half of the acid chloride had been added, the reaction mixture became completely homogenous. Two hours after the addition of the acid chloride, the reaction mixture was heated to reflux and maintained overnight. The solvent was concentrated through the use of a Dean-Stark trap. Cooling to ambient temperature provided a white precipitate, which was collected by filtration. The solid was slurried in 1 L of 1% hot aqueous sodium carbonate (75-80° C.) for 1 hour. The mixture was then cooled in an ice bath and the solid material was filtered, rinsed with water, and dried to yield 22.7 g of 1-[7-benzyloxy-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol as a white solid, mp 170-171.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-cccdbf26dc164696bf7843228c63d267
Source noteuspto-grants-2011_03