HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78613Erstellt: 23. Oktober 2026
Potassium Carbonate → Tert butyl-5-(2-bromophenyl)-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl(tert-butoxycarbonyl)carbamate
https://huagongshe.com/de/reaction/78613
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | (2-Bromophenyl)boronic acid | HCID 2773294 | — |
| Edukt | Tert-butyl N-[5-bromo-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]-N-tert-butoxycarbonyl-carbamate | HCID 59471994 | — |
| Katalysator | Palladium--triphenylphosphane (1/1) | HCID 15220664 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Tert butyl-5-(2-bromophenyl)-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl(tert-butoxycarbonyl)carbamate | HCID 59472100 | — |
Reaktionsschritte
A mixture of (2-bromophenyl)boronic acid (100 mg, 0.4979 mmol), tert-butyl N-[5-bromo-3-(5-phenyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl]-N-tert-butoxycarbonyl-carbamate (258.1 mg, 0.4979 mmol), potassium carbonate (206.5 mg, 1.494 mmol) and triphenylphosphane palladium (13.06 mg, 11.54 μL, 0.04979 mmol) in DMF (3 mL) was heated at 50° C. for 1 h. The reaction mixture was cooled to room temperature and filtered through a Celite,™ pad. The pad was washed with ethyl acetate (1×10 mL) and the combined filtrates were washed with water (2×10 mL) and brine (1×10 mL), dried over MgSO4 and concentrated to leave the product as a solid which was used directly in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841308B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-5aa3b9cc5e2c47e9accd4c77576184eb |
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| Quellennotiz | uspto-grants-2014_09 |
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