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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228682Generated: October 29, 2026

Imidazole → [2-({7-[2-Hydroxy-3-(1-imidazoyl)propoxy]-6-methoxy-4-quinolyl}oxy)-5-methylphenyl](phenyl)methanone

https://huagongshe.com/reaction/228682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant(2-{[6-Methoxy-7-(2-oxiranylmethoxy)-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanoneHCID 57756552—
Product[2-({7-[2-Hydroxy-3-(1-imidazoyl)propoxy]-6-methoxy-4-quinolyl}oxy)-5-methylphenyl](phenyl)methanoneHCID 8660518580%

Reaction Conditions

Temperature80 °C

Reaction Steps

(2-{[6-Methoxy-7-(2-oxiranylmethoxy)-4-quinolyl]oxy}-5-methylphenyl)(phenyl)methanone (39 mg) and imidazole (18 mg) were suspended in N,N-dimethylformamide (3 ml), and the suspension was stirred at 80° C. overnight. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using methanol-chloroform to give the title compound (36 mg, yield 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-ff4c91c27ea6403caf05ba497c8e8757
Source noteuspto-grants-2009_07