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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393642Erstellt: 24. Oktober 2026

Triphenylphosphine → 4-Chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline

https://huagongshe.com/de/reaction/393642

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Edukt1H-1,2,4-Triazole-1-ethanolHCID 550925—
Edukt4-Chloro-6-methoxyquinolin-7-olHCID 135583731—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinolineHCID 2264655445%

Reaktionsschritte

Diethyl azodicarboxylate (1 ml, 6.5 mmol) was added dropwise to a solution of 4-chloro-7-hydroxy-6-methoxyquinoline (845 mg, 4.0 mmol), (prepared as described for the starting material in Example 3), 2-([1,2,4]-triazol-1-yl)ethanol (500 mg, 4.4 mmol), (Ann. Pharm. Fr. 1977, 35, 503-508), and triphenylphosphine (1.7 g, 6.5 mmol) in methylene chloride (40 ml) under argon. After stirring for 4 days at ambient temperature, the insoluble materials were removed by filtration. The volatiles were removed by evaporation and the residue was purified by column chromatography on silica eluting with methylene chloride/acetonitrile/methanol (75/20/5). The product was purified by a second chromatography on neutral alumina eluting with methylene chloride/acetonitrile/methanol (75/20/5). The purified product was triturated with ether, collected by filtration and dried under vacuum to give 4-chloro-6-methoxy-7-(2-([1,2,4]-triazol-1-yl)ethoxy)quinoline (544 mg, 45%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06809097B1
Quelldatensatzuspto-grants-2004_10
ORD IDord-8d3f5f227766422fabf12c317ca2b63e
Quellennotizuspto-grants-2004_10