HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853412Generated: October 30, 2026
Water → 6,7-Dimethoxy-4-(5-indolinyloxy)quinoline
https://huagongshe.com/reaction/853412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-[(1H-Indol-5-yl)oxy]-6,7-dimethoxyquinoline | HCID 22132645 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6,7-Dimethoxy-4-(5-indolinyloxy)quinoline | HCID 22936441 | 79.5% |
Reaction Steps
After dissolving 6,7-dimethoxy-4-(5-indolyloxy)quinoline (30 mg, 0.0780 mmol, described in WO9717329, p.52) in trifluoroacetic acid (0.9 ml), triethylsilane (45 ml, 0.2808 mmol, 3.0 eqM) was added while cooling on ice, and the mixture was stirred for 4 hours and 30 minutes at room temperature under a nitrogen atmosphere. After cooling, the reaction solution was diluted with ethyl acetate, neutralized with saturated sodium bicarnobate water, extracted with ethyl acetate, washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/ethanol system) to obtain the title compound (20 mg, 0.0620 mmol, 66.28%) as light yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253286B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-444f5c4534214b3ab7cfc22a48ec19c9 |
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| Source note | uspto-grants-2007_08 |
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