Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-(4-Methoxyphenyl)ethyl methanesulfonate | HCID 277977 | — |
| Edukt | Norastemizole hydrobromide | HCID 3018631 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Astemizole | HCID 2247 | 48% |
Reaktionsschritte
A mixture of 2.3 parts of 2-(4-methoxyphenyl)ethyl methanesulfonate, 4.9 parts of 1-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-1H-benzimidazol-2-amine dihydrobromide, 3.2 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide is stirred overnight at 70° C. The reaction mixture is poured onto water. The product is extracted with methylbenzene. The extract is washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 2,2'-oxybispropane, yielding 2.2 parts (48%) of 1-(4-fluorophenylmethyl)-N-{1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl}-1H-benzimidazol-2-amine; mp. 172.9° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04219559 |
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| Quelldatensatz | uspto-grants-1980_08 |
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| ORD ID | ord-979daa0708dc452abb8295cefc7b72c8 |
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| Quellennotiz | uspto-grants-1980_08 |
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