HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323510Erstellt: 25. Oktober 2026
Ammonium fluoride → (1-(2-hydroxyethyl)-1H-benzimidazol-2-yl)(1-(ethoxycarbonyl)piperidin-4-yl)amine
https://huagongshe.com/reaction/323510
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium fluoride | HCID 25516 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | (1-(2-(t-butyldimethylsilyloxy)ethyl)-1H-benzimidazol-2-yl)(1-(ethoxycarbonyl)piperidin-4-yl)amine | HCID 22009292 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (1-(2-hydroxyethyl)-1H-benzimidazol-2-yl)(1-(ethoxycarbonyl)piperidin-4-yl)amine | HCID 22009172 | — |
Reaktionsschritte
Combine (1-(2-(t-butyldimethylsilyloxy)ethyl)-1H-benzimidazol-2-yl)(1-(ethoxycarbonyl)piperidin-4-yl)amine (0.53 g, 12 mmol) and ammonium fluoride (2.667 g, 72 mmol) in methanol (60 mL). Heat to about 60° C. After 2.5 hours, cool, evaporate in vacuo and partition the evaporated reaction mixture between dichloromethane and a saturated aqueous sodium bicarbonate solution. Separate the layers and extract the organic layer twice with water and then brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give (1-(2-hydroxyethyl)-1H-benzimidazol-2-yl)(1-(ethoxycarbonyl)piperidin-4-yl)amine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06211199B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-442278bd30b547888e969a8de56d3b47 |
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| Quellennotiz | uspto-grants-2001_04 |
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