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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228959Generated: October 26, 2026

Dimethylformamide → HCID 23078599, compound

https://huagongshe.com/reaction/228959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant7-(2-Chloro-ethoxy)-6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolineHCID 23078272—
SolventWaterHCID 962—
ProductHCID 23078599HCID 2307859989%

Reaction Conditions

Temperature75 °C

Reaction Steps

N,N-Dimethylformamide (1 ml) was added to 7-(2-chloro-ethoxy)-6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinoline (compound 353) (35 mg), potassium carbonate (37 mg), and piperidine (23 mg), and the mixture was stirred at 75° C. overnight. The reaction solution was cooled to room temperature, water was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was then dried over anhydrous magnesium 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 (35 mg, yield 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-8ed2625226c14ea4afdb1b6bc42a90fe
Source noteuspto-grants-2009_07