HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Chlorobenzimidazole → N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Chlorobenzimidazole | HCID 78572 | — |
| Edukt | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Produkt | N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amine | HCID 16640950 | — |
Reaktionsschritte
Combine 2-chloro-1H-benzimidazole (5.0 g, 33 mmol) and 1-benzyl-4-aminopiperidine (14.2 g, 75 mmol) and heat to about 150° C. After 12 hours, cool and partition between water and chloroform, warming if necessary. Separate the layers and add methanol and toluene to the organic layer. Evaporate the organic layer in vacuo to give a solid. Triturate the solid with ethyl acetate, collect by filtration, and dry to give (1H-benzimidazol-2-yl)(1-benzylpiperidin-4-yl)amine: Rf=0.30 (2% triethylamine/10% methanol/ethyl acetate).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06211199B1 |
| Quelldatensatz | uspto-grants-2001_04 |
| ORD ID | ord-560697a9c71444b5a7705a1b92fc2c32 |
| Quellennotiz | uspto-grants-2001_04 |