HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 533402Erstellt: 24. Oktober 2026
3,5-Difluoropyridine → Methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate
https://huagongshe.com/de/reaction/533402
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3,5-Difluoropyridine | HCID 642820 | — |
| Edukt | Methyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylate | HCID 86666251 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate | HCID 67774472 | 20,8% |
Reaktionsschritte
Under argon gas atmosphere, n-butyllithium (1.6 M THF solution, 0.7 mL) was added dropwise to a mixture of 3,5-difluoropyridine (123 mg) and THF (3 mL) at −78° C., followed by stirring at the same temperature for one hour. Then, zinc chloride (146 mg) was added, and stirred for an additional hour. Methyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylate (330 mg) and tetrakis(triphenylphosphine)palladium (206 mg) were added thereto, followed by heating under stirring in an oil bath at 60° C. for 3 hours. The reaction mixture was concentrated under reduced pressure and purified under silica gel column chromatography (hexane/ethyl acetate) to obtain methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate (62 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08853242B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-684a031afcaa4e1b8a4c20dd142e9d36 |
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| Quellennotiz | uspto-grants-2014_10 |
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