HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Nitro-1H-benzimidazole → 2-cyclopropyl-1H-benzimidazol-5-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Nitro-1H-benzimidazole | HCID 97234 | — |
| Edukt | 4-Nitro-1,2-phenylenediamine | HCID 5111791 | — |
| Edukt | 2-cyclopropyl-5-nitro-1H-1,3-benzodiazole | HCID 16227522 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Produkt | 2-cyclopropyl-1H-benzimidazol-5-amine | HCID 18379863 | 75% |
Reaktionsschritte
A solution of 4-nitro-1,2-phenylenediamine (1.0 g, 6.6 mmol) in 15 ml of cyclopropanecarboxylic acid was stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo to yield a oil, which was dissolved in 100 ml of EtOAc and washed with aqueous NaHCO3. Organic layer was dried over MgSO4 and concentrated in vacuo, yielding an oil which was characterized as 2-cyclopropyl-5-nitrobenzimidazole and subjected to a following reaction without further purification. The nitrobenzimidazole and 50 mg of 10% Pd-C were dissolved in 100 ml of MeOH and stirred for 12 h under H2. The reaction mixture was filtered and concentrated in vacuo to provide 0.87 g (4.9 mmol, 75%) of the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06495583B1 |
| Quelldatensatz | uspto-grants-2002_12 |
| ORD ID | ord-08eaca019fa94be39a12b79f84a7b015 |
| Quellennotiz | uspto-grants-2002_12 |