HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227939Generated: October 29, 2026
HCID 18753448, compound → HCID 22478248, compound
https://huagongshe.com/reaction/2227939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18753448 | HCID 18753448 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22478248 | HCID 22478248 | 31% |
Reaction Steps
A solution of OXONE, (trade mark of E.I. duPont de Nemours & Co., Inc), (150 mg) in water (2 ml) was added to a solution of 4-(4-bromo-2-fluoroanilino)-7-(2-ethylthioethoxy)-6-methoxyquinazoline (125 mg, 0.28 mmol), (prepared as described in Example 24), in methanol (10 ml). The reaction mixture was stirred for 16 hours at ambient temperature, the methanol was removed by evaporation, the aqueous residue was basified with sodium hydrogen carbonate solution and then extracted with ethyl acetate (3×30 ml). The extracts were combined, washed with water (×2), and then brine, and dried (MgSO4). The solvent was removed by evaporation and the residue was purified by column chromatography eluting with ethyl acetate and then with methylene chloridetmethanol (9/1) to give 4-(4-bromo-2-fluoroanilino)-7-(2-ethylsulphinylethoxy)-6-methoxyquinazoline (32 mg, 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06414148B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-ab4bb2e0c4f14cc1a7aa001ee8b3c8ce |
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| Source note | uspto-grants-2002_07 |
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