HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280338Erstellt: 24. Oktober 2026
Potassium Iodide → N-[1-[2-(ethenyloxy)ethyl]-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine
https://huagongshe.com/de/reaction/280338
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | 2-Chloroethyl vinyl ether | HCID 8074 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Norastemizole hydrobromide | HCID 3018631 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[1-[2-(ethenyloxy)ethyl]-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine | HCID 13653865 | 32% |
Reaktionsschritte
A mixture of 1.6 parts of 1-chloro-2-(ethenyloxy)ethane, 7.3 parts of 1-(4-fluorophenylmethyl)-N-(4-piperidinyl)-1H-benzimidazol-2-amine dihydrobromide, 3.1 parts of sodium carbonate, 0.1 parts of potassium iodide and 135 parts of N,N-dimethylformamide was stirred and heated overnight at 70° C. The reaction mixture was poured onto water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (96:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 1.9 parts (32%) of N-[1-[2-(ethenyloxy)ethyl]-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine; mp. 138.5° C. (compound 1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04588722 |
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| Quelldatensatz | uspto-grants-1986_05 |
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| ORD ID | ord-eec8b0d9934e41c8810236d0bc8d8b24 |
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| Quellennotiz | uspto-grants-1986_05 |
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