HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167462Erstellt: 26. Oktober 2026
Triphenylphosphine → (5R)-3-(3-fluoro-4-imidazol-1-yl-phenyl)-5-(isoxazol-3-yloxymethyl)oxazolidin-2-one
https://huagongshe.com/reaction/1167462
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Edukt | 3-(3-Fluoro-4-(imidazol-1-yl)phenyl)-5(R)-hydroxymethyloxazolidin-2-one | HCID 10492764 | — |
| Edukt | HCID 178516613 | HCID 178516613 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (5R)-3-(3-fluoro-4-imidazol-1-yl-phenyl)-5-(isoxazol-3-yloxymethyl)oxazolidin-2-one | HCID 497412 | 59,8% |
Reaktionsschritte
3-(3-Fluoro-4-(imidazol-1-yl)phenyl)-5(R)-hydroxymethyloxazolidin-2-one (WO 96/23788; 280 mg, 1 mmol), 3-hydroxyisoxazole (94 mg, 1.1 mmol), and triphenylphosphine (330 mg, 1.25 mmol) were suspended by stirring in dry tetrahydrofuran (10 ml) under nitrogen at ambient temperature. Diisopropylazodicarboxylate (308 mg, 1.5 mmol) was added dropwise over 10 minutes. The suspension dissolved, and stirring was continued at the same temperature for 2 hours. The mixture was evaporated to dryness, and the residue purified by chromatography on a 20 g silica Mega Bond Elut® columns, eluting with a gradient increasing in polarity from 50 to 100% EtOAc in isohexane. Relevant fractions were combined and evaporated to give the desired product (206 mg). MS (ESP): 345 (MH+) for C16H13FN4O4.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06617339B1 |
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| Quelldatensatz | uspto-grants-2003_09 |
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| ORD ID | ord-b3b6251e19af4ef2a1c434e00097a7ce |
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| Quellennotiz | uspto-grants-2003_09 |
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