HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068085Generated: October 26, 2026
Potassium Carbonate → 7-[2-(4-acetylpiperazin-1-yl)ethoxy]-4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinazoline
https://huagongshe.com/reaction/2068085
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-fluoro-2-methyl-1H-indol-5-ol | HCID 10352036 | — |
| Reactant | 7-[2-(4-Acetylpiperazin-1-yl)ethoxy]-4-chloro-6-methoxyquinazoline | HCID 58960240 | — |
| Catalyst | Potassium Carbonate | HCID 11430 | — |
| Catalyst | 4-fluoro-2-methyl-1H-indol-5-ol | HCID 10352036 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 7-[2-(4-acetylpiperazin-1-yl)ethoxy]-4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinazoline | HCID 11752254 | 60.5% |
Reaction Steps
A mixture of 7-[2-(4-acetylpiperazin-1-yl)ethoxy]-4-chloro-6-methoxyquinazoline (12.24 g, 33.5 mmol), 4-fluoro-5-hydroxy-2-methylindole (5.54 g, 33.5 mmol), (prepared as described for the starting material in Example 1), and potassium carbonate (4.64 g, 33.5 mmol) was heated in N,N-dimethylacetamide (150 ml) at 85° C. for 4 hours. 4-Fluoro-5-hydroxy-2-methylindole (33 mg, 0.2 mmol) and potassium carbonate (108 mg, 57%) were added and the mixture heated for a further 1 hour at 85° C. and then stirred at ambient temperature overnight. The mixture was filtered and concentrated under reduced pressure. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5) to give a white solid which was suspended in acetone (150 ml) and heated at reflux for 1 hour. After cooling the mixture was filtered and the solid dried in air to give 7-[2-(4-acetylpiperazin-1-yl)ethoxy]-4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinazoline (10 g, 60%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293902B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-7b91a71fd4c346728152273dc6ea20a6 |
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| Source note | uspto-grants-2012_10 |
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