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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-AnisidineHCID 7732—
EduktMethyl 3-amino-4-phenylthiophene-2-carboxylateHCID 2759782—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
Produkt3-Amino-N-(4-methoxyphenyl)-4-phenylthiophene-2-carboxamideHCID 8672980085,7%

Reaktionsbedingungen

Temperatur120 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09260448B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-9d507646114648c5bd9f984a4ea6a178
Quellennotizuspto-grants-2016_02