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HRID 51110Erstellt: 24. Oktober 2026

(4-Aminophenoxy)benzene → (4-Phenoxyphenyl)-(7-iodoquinolin-4-yl)amine

https://huagongshe.com/de/reaction/51110

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Aminophenoxy)benzeneHCID 8764—
Edukt4-Amino-7-iodoquinolineHCID 3082517—
Edukt4-Chloro-7-iodoquinolineHCID 10589540—
Lösungsmittel1-ButanolHCID 263—
Produkt(4-Phenoxyphenyl)-(7-iodoquinolin-4-yl)amineHCID 21952018—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

4-Chloro-7-iodoquinoline (10 g, 34 mmol) [Semenov, V. P.; Studenikov, A. N. Synthesis of 7-iodo-4-aminoquinoline derivatives. Khim. Geterotsikl. Soedin. (1980), Issue 7, 972-5] and 4-phenoxyaniline (6.38 g, 34 mmol) in butanol (75 ml) were heated at gentle reflux (120° C.) overnight (18 hrs). On cooling the resultant precipitate was collected by filtration and washed with acetonitrile (2×50 ml). The resultant solid was suspended in chloroform (500 ml) and 2N sodium carbonate solution (300 ml) and heated at 75° C. for 45 mins. On cooling the resultant precipitate was collected by filtration, washed with water (2×50 ml) and dried to yield the product as a pale brown solid. (9.95 g, 66%) δH [2H6]DMSO 8.35(3H, m), 8.20(1H, s), 8.10(1H, d), 7.85(1H, s), 7.35(4H, m), 7.15(4H, d), 6.75(1H, d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713485B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-ff57ce611b9046aabc723cc98a9f5ffc
Quellennotizuspto-grants-2004_03