Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Edukt | 3-Methyl-5-(tributylstannyl)isoxazole | HCID 2763255 | — |
| Edukt | 5-Bromo-2-fluoropyridine | HCID 2783168 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Produkt | HCID 58015530 | HCID 58015530 | 54,5% |
Reaktionsschritte
A 48 mL tube was charged with 5-bromo-2-fluoropyridine (1.17 ml, 11.4 mmol), 3-methyl-5-(tributylstannyl)isoxazole (5.29 g, 14.2 mmol), cyclohexyl JohnPhos (0.398 g, 1.14 mmol), Pd2dba3 (0.312 g, 0.341 mmol), and DMF (12.4 ml, 159 mmol), flushed with argon, sealed, then heated at 90° C. for 16 hours. Additional 3-methyl-5-(tributylstannyl)isoxazole (5.29 g, 14.2 mmol) (2 g), Pd2 dba3 (0.312 g, 0.341 mmol), and cyclohexyl JohnPhos (0.398 g, 1.14 mmol) were added and the mixture was stirred at 90° C. for 10 more hours. This was concentrated and the brown residue was purified by MPLC, eluting with 15% ethyl acetate in hexanes isocratic. 2-fluoro-5-(3-methylisoxazol-5-yl)pyridine (1.1029 g, 54.5% yield) isolated as a light yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08198448B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-05945d12f2a2422db148d935ab22bd5d |
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| Quellennotiz | uspto-grants-2012_06 |
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