Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 4-Bromo-1-phenyl-1H-pyrazole | HCID 786811 | — |
| Edukt | Furan-2-boronic acid | HCID 2734357 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | 2-Methylbenzyl alcohol | HCID 6994 | — |
| Produkt | 4-(furan-2-yl)-1-phenyl-1H-pyrazole | HCID 86303659 | 16,7% |
Reaktionsschritte
4-bromo-1-phenyl-1H-pyrazole (140 mg, 0.627 mmol), furan-2-ylboronic acid (88.2 mg, 0.941 mmol), Pd(PPh3)4 (70 mg, 0.062 mmol), and Cs2CO3 (400 mg, 1.254 mmol) were combined in toluene-methanol (1:1) (2 ml). The reaction mixture was heated under microwave at 80° C. for 60 minutes. The reaction mixture was then filtered and washed with toluene-ethanol (5 ml), and the filtrate was concentrated. The crude product was column purified using 15-20% ethyl acetate/hexanes, and was then further purified by preparative HPLC to yield the desired 4-(furan-2-yl)-1-phenyl-1H-pyrazole (22 mg, 0.10 mmol 16.7%). The HPLC purity of the final product was 99.72%. LC-MS [M+H] 211 (C13H10N2O+H expected 211.08). The 1H-NMR spectra was in accordance with the chemical structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09402397B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
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| ORD ID | ord-b3d6cb71d4c345799e8a9583a569bf72 |
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| Quellennotiz | uspto-grants-2016_08 |
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