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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74236Erstellt: 23. Oktober 2026

3-Furaldehyde → 5-(Benzoxazol-2-yl)-2-(furan-3-yl)-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/de/reaction/74236

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-FuraldehydeHCID 10351—
EduktPotassium CarbonateHCID 11430—
EduktPotassium hydroxy sulfiteHCID 23707502—
Edukt5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-(Benzoxazol-2-yl)-2-(furan-3-yl)-1-(tetrahydropyran-4-yl)benzimidazoleHCID 4982145969%

Reaktionsschritte

To a solution of 5-(benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (200 mg, 0.646 mmol) in dimethylformamide (2 mL) was added 3-furaldehyde (80.7 mg, 0.840 mmol) and oxone (258 mg, 0.420 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (171 mg, 69% yield) as pale yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829035B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-3654201990e44b268913e761ca02e6fd
Quellennotizuspto-grants-2014_09