HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1403142Erstellt: 25. Oktober 2026
Ethanol → 1-{4-[({4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(morpholin-4-yl)pyrimidin-2-yl}amino)methyl]piperidin-1-yl}-3-fluoropropan-2-ol
https://huagongshe.com/reaction/1403142
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanol | HCID 702 | — |
| Edukt | 1,2-Epoxy-3-fluoropropane | HCID 10418 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-morpholin-4-yl-N-(piperidin-4-ylmethyl)pyrimidin-2-amine | HCID 86686777 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-{4-[({4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(morpholin-4-yl)pyrimidin-2-yl}amino)methyl]piperidin-1-yl}-3-fluoropropan-2-ol | HCID 86686776 | — |
Reaktionsschritte
To a mixture of 4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-morpholin-4-yl-N-(piperidin-4-ylmethyl)pyrimidin-2-amine (100 mg) and ethanol (2 mL) were added 2-(fluoromethyl)oxirane (19 μL) and N,N-diisopropyl ethylamine (79 μL), and the mixture was stirred in a microwave reactor at 120° C. for 1 hour. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and then the residue was purified by amino silica gel column chromatography (ethyl acetate:hexane) to obtain 1-{4-[({4-[2-(difluoromethyl)-1H-benzimidazol-1-yl]-6-(morpholin-4-yl)pyrimidin-2-yl}amino)methyl]piperidin-1-yl}-3-fluoropropan-2-ol (81 mg) as a white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08912180B2 |
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| Quelldatensatz | uspto-grants-2014_12 |
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| ORD ID | ord-38e3e188e5524b7691b98d0105a36a12 |
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| Quellennotiz | uspto-grants-2014_12 |
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