HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450472Erstellt: 24. Oktober 2026
Aldoxime → 2-Fluoro-4-(2-(3-methylisoxazol-5-yl)pyridin-4-yloxy)benzenamine
https://huagongshe.com/de/reaction/450472
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Aldoxime | HCID 7863 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | 4-(2-Ethynylpyridin-4-yloxy)-2-fluorobenzenamine | HCID 59825583 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Fluoro-4-(2-(3-methylisoxazol-5-yl)pyridin-4-yloxy)benzenamine | HCID 59825581 | 23,1% |
Reaktionsschritte
Acetaldoxime (0.078 g, 1.321 mmol) and triethylamine (0.246 ml, 1.761 mmol) were added to a solution of 4-(2-ethynylpyridin-4-yloxy)-2-fluorobenzenamine (0.201 g, 0.881 mmol) in THF (4 mL) in a microwave reaction vial. To this solution was added 1-chloropyrrolidine-2,5-dione (0.176 g, 1.32 mmol) and the mixture was stirred at 130° C. for 45 min under microwave irradiation. An additional 1.5 eq each of acetaldoxime and 1-chloropyrrolidine-2,5-dione were added and the reaction heated for an additional 45 min at 130° C. This process was repeated one more time. The mixture was poured into a biphasic solution of water (40 mL) and EtOAc (30 mL). The organic layer was separated and the aqueous layer was extracted with EtOAc (2×20 ml). The combined organics were washed with brine, dried (Na2SO4), concentrated in vacuo and purified by column chromatography (EtOAc-hexanes) to afford 2-fluoro-4-(2-(3-methylisoxazol-5-yl)pyridin-4-yloxy)benzenamine (58 mg, 23% yield) as light red colored residue. MS (ESI) m/z: 286.1 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08486951B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-6ae99d6367eb4e3ab7485053c800488d |
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| Quellennotiz | uspto-grants-2013_07 |
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