HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279574Erstellt: 24. Oktober 2026
4-Chloro-2-fluorophenol → 7-Benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline
https://huagongshe.com/de/reaction/279574
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Chloro-2-fluorophenol | HCID 181975 | — |
| Edukt | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline hydrochloride | HCID 22030836 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 7-Benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline | HCID 21874825 | 77% |
Reaktionsschritte
4-Chloro-2-fluoro-phenol (264 mg, 1.8 mmol) was added to a solution of 7-benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (506 mg, 1.5 mmol), (prepared as described for the starting material in Example 1), in pyridine (8 ml) and the mixture heated at reflux for 45 minutes. The solvent was removed by evaporation and the residue partitioned between ethyl acetate and water. The organic layer was washed with 0.1M hydrochloric acid, water and brine, dried (MgSO4) and the solvent removed by evaporation. The solid residue was triturated with petroleum ether and the crude product collected by filtration and purified by flash chromatography eluting with methylene chloride/ether (9/1) to give 7-benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline (474 mg, 77%) as a cream solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06362336B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-8df83238fa9745758f57a2fcb0296b6a |
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| Quellennotiz | uspto-grants-2002_03 |
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