HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Formic Acid → 7-Chloro-1H-benzo[d]imidazol-5-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Formic Acid | HCID 284 | — |
| Edukt | Formamide | HCID 713 | — |
| Edukt | 6-Chloro-2,4-dinitroaniline | HCID 19052 | — |
| Edukt | HCID 178522168 | HCID 178522168 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Acetic Anhydride | HCID 7918 | — |
| Produkt | 7-Chloro-1H-benzo[d]imidazol-5-amine | HCID 178507673 | — |
Reaktionsschritte
Methanolic solution of 6-chloro-2,4-dinitroaniline (2.4 g, 11 mmol) was stirred overnight with 100 mg of 10% Pd/C under H2. Reaction mixture was filtered and concentrated in vacuo to provide an oil which was dissolved in 10 ml of acetic anhydride and 10 ml of formic acid and stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo, yielding a brown oil which was characterized as 4-chloro-6-foramidylbenzimidazole in NMR analysis. The formamide was dissolved in 20 ml of HCl sat'd EtOH and stirred for 3h at 25° C. The reaction mixture was purified in column chromatography (5% MeOH/EtOAc) to provide 0.89 g (5.3 mmol, 48% overall) of the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06316637B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-98b5b6c4ca6e4c908c7280faa5b61774 |
| Quellennotiz | uspto-grants-2001_11 |