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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611766Generated: October 26, 2026

Methanol → 1-(2-{[3-(3,4-dimethylphenyl)-2-propynyl]oxy}ethyl]-1H-imidazo[4,5-c]quinolin-4-amine

https://huagongshe.com/reaction/1611766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyrrolidineHCID 31268—
Reactant4-Iodo-1,2-dimethylbenzeneHCID 141646—
Reactant1-[2-(2-propynyloxy)ethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 9856610—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventChloroformHCID 6212—
Product1-(2-{[3-(3,4-dimethylphenyl)-2-propynyl]oxy}ethyl]-1H-imidazo[4,5-c]quinolin-4-amineHCID 2225446314.2%

Reaction Steps

Under a nitrogen atmosphere, 1-[2-(2-propynyloxy)ethyl]-1H-imidazo[4,5-c]quinolin-4-amine (0.5 g, 1.9 mmol), copper (I) iodide (0.036 g, 0.2 mmol), 4-iodo-ortho-xylene (0.5 g, 2.1 mmol) and pyrrolidine (10 mL) were combined and stirred at ambient temperature. Dichlorobis(triphenylphosphine)palladium(II) (0.066 g, 0.1 mmol) was added and the reaction mixture was stirred at ambient temperature for 1 hour. Analysis by TLC (30% methanol in chloroform) indicated that starting material was still present. The reaction mixture was heated at 65° C. overnight. The pyrrolidine was removed under reduced pressure. The resulting residue was triturated with dichloromethane containing methanol. The insoluble material was isolated by filtration and then recrystallized from toluene (40 mL) to provide 0.1 g of 1-(2-{[3-(3,4-dimethylphenyl)-2-propynyl]oxy}ethyl]-1H-imidazo[4,5-c]quinolin-4-amine as a solid, m.p. 214-216° C. Analysis: Calculated for C23H22N4O: % C, 74.57; % H, 5.99; % N, 15.12; Found: % C, 74.24; % H, 5.98; % N, 15.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989389B2
Source datasetuspto-grants-2006_01
ORD IDord-87d42cfb3d0e4b14a7e99258433d8f4e
Source noteuspto-grants-2006_01