HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl iodide → 4-({2-[(4-bromophenyl)amino]-1-methyl-1H-1,3-benzodiazol-6-yl}oxy)-N-methylpyridine-2-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | 4-Bromophenyl isothiocyanate | HCID 16133 | — |
| Edukt | {4-[4-Amino-3-(methylamino)phenoxy](2-pyridyl)}-n-methylcarboxamide | HCID 58385469 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-({2-[(4-bromophenyl)amino]-1-methyl-1H-1,3-benzodiazol-6-yl}oxy)-N-methylpyridine-2-carboxamide | HCID 22040978 | — |
Reaktionsbedingungen
| Temperatur | 60 °C |
|---|
Reaktionsschritte
A solution of the {4-[4-amino-3-(methylamino)phenoxy](2-pyridyl)}-N-methyl-carboxamide(1 eq) in methanol was treated with 4-bromophenylisothiocyanate (1 eq) and stirred at 60° C. for 2 hours. The reaction mixture was cooled down to room temperature and iodomethane (1 eq) was added and stirred overnight at 60° C. The reaction was concentrated and preparative chromatography gave (4-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-6-yloxy}-(2-pyridyl)-N-methylcarboxamide. MS: MH+=452.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07071216B2 |
| Quelldatensatz | uspto-grants-2006_07 |
| ORD ID | ord-204e0e7bf12a4fd99666168d14b4e1c1 |
| Quellennotiz | uspto-grants-2006_07 |