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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Dichloro-6,7-dimethoxyquinazolineHCID 520327—
EduktNitronium tetrafluoroborateHCID 11073463—
LösungsmittelAcetonitrileHCID 6342—
Produkt2,4-Dichloro-6,7-dimethoxy-5-nitroquinazolineHCID 2270704874%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750214B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-1d53f366d6aa40a38022f11709a45a87
Quellennotizuspto-grants-2004_06