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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1791616Erstellt: 26. Oktober 2026

Triphenylphosphine → 4-(2-Methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazoline

https://huagongshe.com/reaction/1791616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt1-PyrrolidinepropanolHCID 209342—
Edukt7-Hydroxy-4-(2-methylindol-5-yloxy)quinazolineHCID 135763114—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-Methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazolineHCID 2203082335,8%

Reaktionsschritte

Diisopropyl azodicarboxylate (146 mg, 0.72 mmol) was added to a solution of 7-hydroxy-4-(2-methylindol-5-yloxy)quinazoline (100 mg, 0.34 mmol), triphenyl phosphine (189 mg, 0.72 mol), and 3-pyrrolidinopropan-1-ol (89 mg, 0.686 mmol), (J. Org. Chem. 1988, 53, 3164), in methylene chloride (2.5 ml). After stirring overnight at ambient temperature, the solid was filtered. The filtrate was purified by column chromatography eluting with ethyl acetate/methylene chloride (1/1) followed by ethyl acetate/methylene chloride/methanol (4/5/1), methylene chloride/methanol (9/1) and 3N ammonia in methanol/methylene chloride (1/9). After removal of the solvent, the residue was triturated with ether, filtered, and dried under vacuum to give 4-(2-methylindol-5-yloxy)-7-(3-(pyrrolidin-yl)propoxy)quinazoline (49 mg, 35%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07074800B1
Quelldatensatzuspto-grants-2006_07
ORD IDord-dc11ca25b1654c81a392193d4382e978
Quellennotizuspto-grants-2006_07