HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl iodide → 1-methyl-1H-1,3-benzodiazol-5-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | 5-Nitrobenzimidazole | HCID 7195 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Chloroform methanol | HCID 21584188 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-methyl-1H-1,3-benzodiazol-5-amine | HCID 315499 | 21% |
| Produkt | 1-Methyl-1H-benzimidazol-6-amine | HCID 13680283 | 11% |
Reaktionsschritte
A solution of 5-nitrobenzimidazole (3.0 g, 18.4 mmol) in 100 ml of THF was stirred with NaH (2.7 g, 36.8 mmol) for 0.5 h at 25° C. To the solution was added methyl iodide (2.0 ml, 20.3 mmol) and resulting mixture was stirred for 12 h. The reaction mixture was concentrated in vacuo to provide an oil, which was dissolved in 200 ml of MeOH and stirred with 0.3 g of 10% Pd/C under H2 for 12 h. The reaction mixture was filtered and concentrated in vacuo, yielding a dark oily residue which was subjected to column chromatography (3% MeOH/CHCl3) to provide 0.69 g (3.9 mmol, 21%) of 1-methyl-5-aminobenzimidazole and 0.36 g (2.0 mmol, 11%) of 3-methyl-5-aminobenzimidazole.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06316637B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-27d1e517041d4ae195c0e0a0f32a5ef1 |
| Quellennotiz | uspto-grants-2001_11 |