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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Propyl 3-(7-benzyloxy-6-methoxy-quinolin-4-yloxy)naphthalene-2-carboxylate | HCID 23078401 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Propyl 3-(7-hydroxy-6-methoxy-quinolin-4-yloxy)-naphthalene-2-carboxylate | HCID 135854829 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-9ec4bdb0fe67400fa6ce02fc482266c4 |
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| Source note | uspto-grants-2009_07 |
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