HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353043Erstellt: 24. Oktober 2026
2,4-Dichloro-6,7-dimethoxyquinazoline → 2,4-Dichloro-6,7-dimethoxy-5-nitroquinazoline
https://huagongshe.com/de/reaction/353043
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,4-Dichloro-6,7-dimethoxyquinazoline | HCID 520327 | — |
| Edukt | Nitronium tetrafluoroborate | HCID 11073463 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2,4-Dichloro-6,7-dimethoxy-5-nitroquinazoline | HCID 22707048 | 74% |
Reaktionsschritte
To a suspension of 2,4-dichloro-6,7-dimethoxyquinazoline (30.0 g, 0.12 mol) in acetonitrile (550 ml) at 0° C. was added nitronium tetrafluoroborate (25.9 g, 0.19 mol) portionwise over 15 min. The reaction was stirred for 0.75 h and then evaporated under reduced pressure. The resulting solid was suspended in a mixture of saturated aqueous sodium bicarbonate and EtOAc and the solid filtered, dissolved in CH2Cl2, dried over MgSO4 and evaporated to give the subtitle compound as a pale yellow solid (27 g). Further material was obtained by separating the organic layer of the filtrate, washing with H2O (1×), saturated brine (1×), drying over MgSO4 and filtering through a pad of silica. Subsequent evaporation under reduced pressure, trituration with EtOAc and filtration gave the subtitle compound as a pale yellow solid (3.9 g, overall yield 88%). Rf 0.24 (ether/hexane 1/1, v/v).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06750214B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-1d53f366d6aa40a38022f11709a45a87 |
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| Quellennotiz | uspto-grants-2004_06 |
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