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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338189Erstellt: 24. Oktober 2026

Cesium carbonate → 9-Fluoro-6-phenanthridinamine

https://huagongshe.com/de/reaction/338189

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
EduktAmantadine HydrochlorideHCID 64150—
Edukt2-Chloro-4-fluorobenzonitrileHCID 109000—
Edukt2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734652—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt9-Fluoro-6-phenanthridinamineHCID 112528283.082,6%

Reaktionsschritte

To a solution of 2-chloro-4-fluorobenzonitrile (1.0 g, 6.42 mmol), 2-aminophenylboronic acid pinacol ester (1.6 g, 7.1 mmol), palladium(II) acetate (0.07 g, 0.32 mmol), amantadine hydrochloride (0.24 g, 1.3 mmol) and cesium carbonate (4.6 g, 14.1 mmol) were added to dioxane previously deaerated with nitrogen and heated to reflux for 17 hours. After cooling, both distilled water and methylene chloride (50 mL) were added to the reaction mixture. The solvent layer was separated and concentrated to give a crude oil that was purified by column chromatography by first using 1:1 ethyl acetate and hexanes ratio followed by 4:1 ethyl acetate/hexanes as the eluants. The pure product was collected to give 9-fluoro-6-phenanthridinamine (42 g, 32% Yield) whose NMR spectrum is consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889864B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-f33504768f854612ad3dd57118648f0e
Quellennotizuspto-grants-2014_11