HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 595939Erstellt: 23. Oktober 2026
1,2-Dimethoxyethane → Methyl 4-(2-aminopyridin-3-yl)-2-fluorobenzoate
https://huagongshe.com/de/reaction/595939
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-Amino-3-bromopyridine | HCID 817700 | — |
| Edukt | 3-Fluoro-4-(methoxycarbonyl)benzeneboronic acid | HCID 2782818 | — |
| Katalysator | HCID 178418807 | HCID 178418807 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Methyl 4-(2-aminopyridin-3-yl)-2-fluorobenzoate | HCID 118046154 | 79% |
Reaktionsschritte
To 3-bromopyridin-2-amine (5 g, 28.9 mmol) in 500 mL round bottom flask was added (3-fluoro-4-(methoxycarbonyl)phenyl)boronic acid (7.44 g, 37.6 mmol), PdCl2(dppf)-DCM (2.115 g, 2.89 mmol), DME (108 mL) and 2M Na2CO3 solution (36.1 mL). The reaction mixture was heated in an oil bath at 110° C. for 4 h. The reaction mixture was diluted with EtOAc and washed with water three times, dried over Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography eluting with 0-100% of EtOAc (containing 10% of MeOH)/heptane yielding 5.6 g of methyl 4-(2-aminopyridin-3-yl)-2-fluorobenzoate in 79% yield. LCMS (m/z): 247.1 (MH+), 0.50 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242996B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-8974d23a49d24df49ab13feee8f313c8 |
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| Quellennotiz | uspto-grants-2016_01 |
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