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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775603Generated: October 26, 2026

P-Anisidine → 3-Amino-N-(4-methoxyphenyl)-4-phenylthiophene-2-carboxamide

https://huagongshe.com/reaction/1775603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantMethyl 3-amino-4-phenylthiophene-2-carboxylateHCID 2759782—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
Product3-Amino-N-(4-methoxyphenyl)-4-phenylthiophene-2-carboxamideHCID 8672980085.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260448B2
Source datasetuspto-grants-2016_02
ORD IDord-9d507646114648c5bd9f984a4ea6a178
Source noteuspto-grants-2016_02