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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132006Erstellt: 23. Oktober 2026

Diiodomethane → 4-[1-(3,4-Dimethylphenoxymethyl)-1H-benzimidazol-2-yl]-furazan-3-yl-N-(2-cyanoethyl)-amine

https://huagongshe.com/de/reaction/132006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiiodomethaneHCID 6346—
Edukt3,4-DimethylphenolHCID 7249—
EduktPotassium CarbonateHCID 11430—
Edukt3-[4-(1H-Benzoimidazol-2-yl)-furazan-3-ylamino]-propionitrileHCID 136389313—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-[1-(3,4-Dimethylphenoxymethyl)-1H-benzimidazol-2-yl]-furazan-3-yl-N-(2-cyanoethyl)-amineHCID 67463629—

Reaktionsschritte

A suspension of 4-(1H-benzimidazol-2-yl)-furazan-3-yl-N-(2-cyanoethyl)-amine (0.15 g, 0.59 mmol, Example 6a), potassium carbonate (0.325 g, 2.36 mmol), diiodomethane (0.16 g, 0.59 mmol) and 3,4-dimethylphenol (0.072 g, 0.59 mmol) in DMF (5 ml) is stirred at room temperature for 16 hours. The reaction mixture is diluted with ethyl acetate, washed with water and dried over sodium sulphate. Filtration of the sodium sulphate, concentration of the filtrate under reduced pressure and chromatography of the residue on silicagel using hexane-ethyl acetate as eluent gives the title compound as a yellowish solid, m.p. 132-135° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07385061B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-32189c7fc33341d3ba13f3040b35987d
Quellennotizuspto-grants-2008_06