HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228531Generated: October 30, 2026
Water → 6,7-Dimethoxy-4-[(1-acetyl-5-indolyl)oxy]quinoline
https://huagongshe.com/reaction/228531
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-[(1H-Indol-5-yl)oxy]-6,7-dimethoxyquinoline | HCID 22132645 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6,7-Dimethoxy-4-[(1-acetyl-5-indolyl)oxy]quinoline | HCID 57756512 | 41% |
Reaction Steps
6,7-Dimethoxy-4-[(1H-5-indolyl)oxy]quinoline (50 mg) was dissolved in N,N-dimethylformamide (1 ml), and 60% sodium hydride (7 mg) was added to the solution, followed by stirring under ice cooling for 30 min. Acetyl chloride (16.6 μl) was added to the reaction solution, and the mixture was stirred under ice cooling for additional one hr. Further, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using methanol-chloroform to give the title compound (23 mg, yield 41%).
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-446f9ce836eb45f4a0ce4807a8401c00 |
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| Source note | uspto-grants-2009_07 |
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