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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727862Generated: October 31, 2026

Water → (4-Tert-butylphenyl)-{4-[6-methoxy-7-(1-propylpiperidin-4-ylmethoxy)quinolin-4-yloxy]phenyl}amine

https://huagongshe.com/reaction/1727862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromopropaneHCID 7840—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Tert-butylphenyl)-{4-[6-methoxy-7-(4-piperidinylmethoxy)-4-quinolyloxy]phenyl}amineHCID 69055371—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(4-Tert-butylphenyl)-{4-[6-methoxy-7-(1-propylpiperidin-4-ylmethoxy)quinolin-4-yloxy]phenyl}amineHCID 575676087%

Reaction Steps

(4-Tert-butylphenyl)-{4-[6-methoxy-7-(4-piperidinylmethoxy)-4-quinolyloxy]phenyl}amine (150 mg) was dissolved in N,N-dimethylformamide (3 ml) to prepare a solution. Potassium carbonate (300 mg) and 1-bromopropane (0.15 ml) were then added to the solution, and the mixture was stirred at room temperature for 4 hr. Water and ethyl acetate were added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and was dried over sodium sulfate. The solvent was removed by evaporation under the reduced pressure, and the residue was purified by thin-layer chromatography on silica gel using chloroform/acetone for development to give the title compound (12 mg, yield 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495104B2
Source datasetuspto-grants-2009_02
ORD IDord-66769e3d155e4d3daace0889219cb3b3
Source noteuspto-grants-2009_02