Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228919Generated: October 25, 2026

Methanesulfonic Acid → Propyl 3-(7-hydroxy-6-methoxy-quinolin-4-yloxy)-naphthalene-2-carboxylate

https://huagongshe.com/reaction/228919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantPropyl 3-(7-benzyloxy-6-methoxy-quinolin-4-yloxy)naphthalene-2-carboxylateHCID 23078401—
SolventTrifluoroacetic acidHCID 6422—
ProductPropyl 3-(7-hydroxy-6-methoxy-quinolin-4-yloxy)-naphthalene-2-carboxylateHCID 13585482968%

Reaction Conditions

Temperature70 °C

Reaction Steps

Propyl 3-(7-benzyloxy-6-methoxy-quinolin-4-yloxy)naphthalene-2-carboxylate (160 mg) was dissolved in trifluoroacetic acid (1.5 ml) to prepare a solution. Methanesulfonic acid (0.15 ml) was added to the solution, and the mixture was stirred at 70° C. for one hr. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. An aqueous sodium hydrogencarbonate solution was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with saturated brine and was 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-acetone to give propyl 3-(7-hydroxy-6-methoxy-quinolin-4-yloxy)-naphthalene-2-carboxylate (87 mg, yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-9ec4bdb0fe67400fa6ce02fc482266c4
Source noteuspto-grants-2009_07