HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 884910Erstellt: 26. Oktober 2026
Dimethylformamide → 2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole
https://huagongshe.com/reaction/884910
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Bromocyclopentane | HCID 8728 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-[5-(Trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol | HCID 136331268 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole | HCID 66880220 | 83,3% |
Reaktionsschritte
To a mixture of 0.28 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 0.28 g of potassium carbonate and 2 ml of DMF, a mixture of 0.29 g of cyclopentyl bromide and 2 ml of DMF was added at room temperature. The reaction mixture was stirred while heating at 60° C. for four hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.29 g of 2-(3-cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 115”).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08242133B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-82f6d84fa98e4abdaaf292cf4423a8cf |
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| Quellennotiz | uspto-grants-2012_08 |
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