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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1170144Erstellt: 25. Oktober 2026

2-Methyl-benzofuran-7-ylamine → 3,5-Difluoro-N-[2-(2-methyl-benzofuran-7-ylamino)-quinolin-5-yl]-benzenesulfonamide

https://huagongshe.com/reaction/1170144

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-benzofuran-7-ylamineHCID 3157485—
EduktN-(2-chloro-quinolin-5-yl)-3,5-difluoro-benzenesulfonamideHCID 86619497—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3,5-Difluoro-N-[2-(2-methyl-benzofuran-7-ylamino)-quinolin-5-yl]-benzenesulfonamideHCID 24988967—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

N-(2-Chloro-quinolin-5-yl)-3,5-difluoro-benzenesulfonamide (150 mg, 0.423 mmol) was dissolved in 3 mL dioxane. Argon was bubbled through the solution for 2 minutes to remove oxygen. (2-Methyl-1-benzofuran-7-yl)amine (245 mg, 1.33 mmol), sodium tert.-butylate (230 mg, 2.40 mmol), 1,1′-bis(diphenylphosphin)ferrocen (36 mg, 0.06 mmol) and 1,1′-bis(diphenylphosphin)ferrocen-palladium(II)chloride (17 mg, 0.02 mmol) were added. The reaction mixture was stirred in a sealed tube at 100° C. for 16 h. The solvent was evaporated and the residue purified by flash chromatography on silica gel (heptane/ethyl acetate 100:0->60:40 gradient). The title compound was obtained as a light brown solid (164 mg, 83%), MS: m/e=466.0 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07825253B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-123b2c376a72419bbe4f04164744dcf8
Quellennotizuspto-grants-2010_11