HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 369035Erstellt: 24. Oktober 2026
Sodium Carbonate → 6-(4-Carboxyphenyl)-8-methoxy-1,7-naphthyridine
https://huagongshe.com/de/reaction/369035
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 4-Carboxyphenylboronic Acid | HCID 312183 | — |
| Edukt | 6-Trifluoromethylsulfonyloxy-8-methoxy-1,7-naphthyridine | HCID 23284635 | — |
| Katalysator | Tri-o-tolylphosphine | HCID 80271 | — |
| Katalysator | 1,5-Diphenylpenta-1,4-dien-3-one;palladium | HCID 154270 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 6-(4-Carboxyphenyl)-8-methoxy-1,7-naphthyridine | HCID 23284642 | 80,8% |
Reaktionsschritte
To a solution of 6-trifluoromethylsulfonyloxy-8-methoxy-1,7-napthyridine (1.5 g, 4.86 mmol) in DMF (40 ml) is added 4-carboxy-phenylboronic acid (0.866 g, 5.34 mmol), bis(dibenzylidenacetone) palladium (112 mg, 0.167 mmol), tri-o-tolylphosphine (96 mg, 0.32 mmol) and aqueous Na2CO3 (14.6 ml, 2N,). The reaction mixture is stirred at 110° for 3 h. The hot solution is filtred through cellit and the solution evaporated to dryness. The crude product is dissolved in hot water (60 ml) and the water phase washed with ethyl acetate (3×50 ml). The product is precipitated from the water phase by carefully adding aqueous HCl (2N, 6 ml). The suspension is filtered and the crude product is stirred again in hot ethyl acetate (50 ml). The cold suspension is filtered to yield the title compound (1.10 g). M+280; Melting point >300°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06136821 |
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| Quelldatensatz | uspto-grants-2000_10 |
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| ORD ID | ord-449fc1ba55304cbb90163e63a52ba620 |
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| Quellennotiz | uspto-grants-2000_10 |
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