HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17435Erstellt: 24. Oktober 2026
1-methyl-2-(tributylstannyl)-1H-pyrrole → 7-fluoro-5-methyl-2-(1-methyl-1H-pyrrol-2-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrile
https://huagongshe.com/de/reaction/17435
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-methyl-2-(tributylstannyl)-1H-pyrrole | HCID 2769397 | — |
| Edukt | 2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 51041429 | — |
| Edukt | 2,6-Di-t-butylcresol | HCID 66637192 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 7-fluoro-5-methyl-2-(1-methyl-1H-pyrrol-2-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 51039965 | — |
Reaktionsschritte
Tributylstannyl-1-methylpyrrole (389 mg, 1.05 mmol), bis(triphenylphosphine)palladium(II) dichloride (49 mg, 0.07 mmol), and a catalytic amount of 2,6-di-tert-butylcresol (2 mg) were added to a toluene (20 ml) solution of 2-chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile (I-130) (200 mg, 0.70 mol), followed by stirring under heat under nitrogen atmosphere for 3 hours. After cooling, the reaction liquid was filtered, and the solvent of the filtrate was evaporate away under reduced pressure. The resulting residue was subjected to silica gel column chromatography, and eluted with a mixed solvent of n-hexane/ethyl acetate (9:1, v/v→5:1, v/v) to obtain a main product. After washing with isopropyl ether, the entitled compound (50 mg, 22%) was collected by filtration as a pale yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737166B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-2d23f605678b474eaf1831fc88ee31f9 |
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| Quellennotiz | uspto-grants-2010_06 |
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