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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228955Generated: October 26, 2026

Sodium Iodide → {2-[6-Methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethyl}-dimethyl-amine

https://huagongshe.com/reaction/228955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant7-(2-Chloro-ethoxy)-6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolineHCID 23078272—
SolventWaterHCID 962—
Product{2-[6-Methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethyl}-dimethyl-amineHCID 5775646133%

Reaction Conditions

Temperature80 °C

Reaction Steps

N,N-Dimethylformamide (2.5 ml) was added to 7-(2-chloro-ethoxy)-6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinoline (compound 353) (100 mg), potassium carbonate (500 mg), sodium iodide (20 mg), and water (0.05 ml), and the mixture was stirred at 80° C. for 3 days. The solvent was removed by distillation under the reduced pressure, water was added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-methanol to give the title compound (34.2 mg, yield 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-cb3e98300b9847bab766862719aa798f
Source noteuspto-grants-2009_07