HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1775603Erstellt: 26. Oktober 2026
P-Anisidine → 3-Amino-N-(4-methoxyphenyl)-4-phenylthiophene-2-carboxamide
https://huagongshe.com/reaction/1775603
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | P-Anisidine | HCID 7732 | — |
| Edukt | Methyl 3-amino-4-phenylthiophene-2-carboxylate | HCID 2759782 | — |
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3-Amino-N-(4-methoxyphenyl)-4-phenylthiophene-2-carboxamide | HCID 86729800 | 85,7% |
Reaktionsschritte
p-Anisidine (29 mg, 0.24 mmol) was dissolved in toluene (2 ml) in a reaction vessel, and trimethylaluminum (2 M in TIIF, 0.12 ml) was added thereto at 0° C. After stirring for 10 min, to the mixture was added methyl 3-amino-4-phenylthiophene-2-carboxylate (50 mg, 0.21 mmol). The resulting mixture was heated to reflux at 120° C. for 16 hr. The completion of the reaction was confirmed by TLC. The reaction mixture was allowed to cool to room temperature, extracted with EtOAc, dried over anhydrous MgSO4, and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (hexane:EtOAc=5:1) to give (57 mg, 0.18 mmol, 84% yield) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09260448B2 |
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| Quelldatensatz | uspto-grants-2016_02 |
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| ORD ID | ord-9d507646114648c5bd9f984a4ea6a178 |
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| Quellennotiz | uspto-grants-2016_02 |
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