HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-hydrazinyl-1-methyl-1H-1,3-benzodiazole → 1-(3-Isoquinolinyl)-1-ethanone-1-(1-methyl-1H-benzo[d]imidazol-2-yl)-hydrazone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-hydrazinyl-1-methyl-1H-1,3-benzodiazole | HCID 1522265 | — |
| Edukt | 1-(Isoquinolin-3-yl)ethan-1-one | HCID 11275275 | — |
| Katalysator | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 1-(3-Isoquinolinyl)-1-ethanone-1-(1-methyl-1H-benzo[d]imidazol-2-yl)-hydrazone | HCID 396600 | — |
Reaktionsschritte
A mixture of 3-acetylisoquinoline (1.01 g, 5.9 mmol) and 1-methyl-2-hydrazinobenzimidazole (0.96 g, 5.55 mmol) in 15 ml of methanol is stirred for approximately 7 days at room temperature after the addition of 5 drops of glacial acetic acid. The reaction is monitored by means of thin layer chromatography (Polygram Sil G/UV254 prefabricated foils; eluting agent: petroleum ether:ethyl acetate (3:7)). The reaction mixture is stored over night in the freezer at approximately −20° C. The precipitate is filtered, washed with ether and dried. The product is recrystallized from a mixture of ethylacetate and petroleum ether. Yield: 1.66 g (95% of theory).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07112680B2 |
| Quelldatensatz | uspto-grants-2006_09 |
| ORD ID | ord-c6fee03aebd242f09f4ca43a817170d2 |
| Quellennotiz | uspto-grants-2006_09 |