HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165920Erstellt: 25. Oktober 2026
Sodium Hydroxide → Ethyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamate
https://huagongshe.com/reaction/1165920
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-(4-Fluorobenzyl)-2-chlorobenzimidazole | HCID 3020241 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | Ethyl piperidin-4-ylcarbamate hydrochloride | HCID 19861299 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamate | HCID 15595031 | — |
Reaktionsschritte
19 g (0.09 mole) of ethyl 4-piperidylcarbamate hydrochloride is solubilized in 120 ml of methanol and neutralized with 17.2 ml of 5.3N sodium methylate. The mixture is filtered and the filtrate evaporated to dryness. The evaporation residue is then mixed with 21.6 g (0.083 mole) of 2-chloro-1-[(4-fluorophenyl)methyl]-1H-benzimidazole and heated to 140° C. for 5 hours. The reaction mass is taken up with methylene chloride and alkalinized with 2N sodium hydroxide. The organic phase is washed with water, dried, filtered and evaporated. The oil obtained is chromatographed on silica (eluent: methylene chloride/methanol, 97.5:2.5). Ethyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamate is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04912219 |
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| Quelldatensatz | uspto-grants-1990_03 |
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| ORD ID | ord-571380de5f4c497b8cb3777447036cb8 |
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| Quellennotiz | uspto-grants-1990_03 |
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