HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Diiodomethane → 4-[1-(3,4-Dimethylphenoxymethyl)-1H-benzimidazol-2-yl]-furazan-3-yl-N-(2-cyanoethyl)-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Diiodomethane | HCID 6346 | — |
| Edukt | 3,4-Dimethylphenol | HCID 7249 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-[4-(1H-Benzoimidazol-2-yl)-furazan-3-ylamino]-propionitrile | HCID 136389313 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-[1-(3,4-Dimethylphenoxymethyl)-1H-benzimidazol-2-yl]-furazan-3-yl-N-(2-cyanoethyl)-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07385061B2 |
| Quelldatensatz | uspto-grants-2008_06 |
| ORD ID | ord-32189c7fc33341d3ba13f3040b35987d |
| Quellennotiz | uspto-grants-2008_06 |