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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 639961Erstellt: 24. Oktober 2026

Triphenylphosphine → 4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazoline

https://huagongshe.com/de/reaction/639961

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt3-Chloro-1-propanolHCID 12313—
EduktDi-tert-butyl azodicarboxylateHCID 97268—
Edukt4-Chloro-6-methoxyquinazolin-7-olHCID 135742251—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazolineHCID 5744722791%

Reaktionsschritte

Triphenylphosphine (2.6 g, 10.1 mmol) and 3-chloropropanol (0.69 ml, 8.2 mmol) were added to a suspension of 4-chloro-7-hydroxy-6-methoxyquinazoline (1.65 g, 7.8 mmol) in dichloromethane (100 ml) under argon. The flask was placed in a water bath at 20° C. and di-tertbutyl azodicarboxylate (2.30 g, 10.1 mmol) added portion wise over a few minutes. The reaction mixture was stirred at ambient temperature for 2 hours. The reaction mixture was concentrated and the solution loaded directly onto a silica chromatography column. Elution with ethyl acetate:petroleum ether (3:7), yielded 4-chloro-7-(3-chloropropoxy)-6-methoxyquinazoline (2.0 g, 91% yield):

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07691867B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-eb7626e449e04f46aadfe370377ff9e0
Quellennotizuspto-grants-2010_04