HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386264Generated: October 30, 2026
Sodium hydride → 4-(5-Fluoro-1-diethoxymethyloxindol-3-yl)-6-methoxy-7-(2-methoxyethoxy)quinazoline
https://huagongshe.com/reaction/1386264
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-6-methoxy-7-(2-methoxyethoxy)quinazoline | HCID 10730653 | — |
| Reactant | HCID 21717300 | HCID 21717300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-Fluoro-1-diethoxymethyloxindol-3-yl)-6-methoxy-7-(2-methoxyethoxy)quinazoline | HCID 21717215 | 75.4% |
Reaction Steps
Sodium hydride (95 mg of a 60% suspension in paraffin oil, 2.4 mmol) was added to a solution of 5-fluoro-1-diethoxymethyloxindole (520 mg, 2.05 mmol) and 4-chloro-6-methoxy-7-(2-methoxyethoxy)quinazoline (220 mg, 0.82 mmol), (prepared as described for the starting material in Example 2), in THF (20 ml). After stirring for 2 hours at ambient temperature, the volatiles were removed by evaporation. The residue was partitioned beween methylene chloride and water, the organic layer was washed with water and then brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using an increasingly polar mixture of methylene chloride/ethyl acetate (100/0 to 0/100) as eluent to give 4-(5-fluoro-1-diethoxymethyloxindol-3-yl)-6-methoxy-7-(2-methoxyethoxy)quinazoline (300 mg, 68%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265411B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-2746c5b8d7374e8ab8371342bbdf784c |
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| Source note | uspto-grants-2001_07 |
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