HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 623783Erstellt: 24. Oktober 2026
Lithium Hydroxide → 1-Benzyl-N,4-dimethyl-N-neopentyl-3-(4-(2,2,2-trifluoroethoxy)phenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxamide
https://huagongshe.com/de/reaction/623783
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-Bromo-4-(2,2,2-trifluoroethoxy)benzene | HCID 22913883 | — |
| Edukt | 1-benzyl-N,4-dimethyl-N-neopentyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxamide | HCID 86711869 | — |
| Katalysator | HCID 178418851 | HCID 178418851 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-Benzyl-N,4-dimethyl-N-neopentyl-3-(4-(2,2,2-trifluoroethoxy)phenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxamide | HCID 86711868 | 89,7% |
Reaktionsschritte
Under an nitrogen atmosphere 1-benzyl-N,4-dimethyl-N-neopentyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxamide (106 mg, 0.216 mmol) was dissolved in DMF (1 mL) and LiOH (4 mg, 0.216 mmol), bis(tri-tert-butylphosphine)palladium (0) (6 mg, 0.014 mmol) and 1-bromo-4-(2,2,2-trifluoroethoxy)benzene (50 mg, 0.196 mmol) were subsequently added. The reaction mixture was stirred at 80° C. under microwave irridation for 1 h. The mixture was cooled to RT and the reaction was stopped by addition of 1M NaOH solution (2 mL). The crude product was extracted with EtOAc (2×3 mL) and the combined organic layers were washed with water (3×1 mL), dried over Na2SO4, filtered and the solvent was removed under reduced pressure. The crude mass was purified by flash chromatography to give SC-260 (95 mg, 89.7%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09302988B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-193d210bbf4f41e9aa40e1f8946886ab |
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| Quellennotiz | uspto-grants-2016_04 |
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