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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248675Erstellt: 25. Oktober 2026

3-Amino-4-methylbenzoic acid → 3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-4-methylbenzoic acid

https://huagongshe.com/reaction/248675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Amino-4-methylbenzoic acidHCID 75568—
Edukt2-Acetylthiomethyl-3-phenyl-propionyl chlorideHCID 10377734—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-4-methylbenzoic acidHCID 1567016952,4%

Reaktionsschritte

3-Amino-4-methylbenzoic acid (1.5 g) is dissolved in a solution of sodium hydrogen carbonate (1.68 g) in water (25 ml), and to the mixture is added dropwise a solution of 2-acetylthiomethyl-3-phenylpropionyl chloride (2.86 g) in tetrahydrofuran (8 ml) with vigorously stirring, and the mixture is stirred at room temperature for 3 hours. Tetrahydrofuran is distilled off at a low temperature under reduced pressure, and the residue is washed with diethyl ether and acidified with hydrochloric acid, and the resulting oily substance is extracted with ethyl acetate. The extract is washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then the solvent is distilled off under reduced pressure. The oily residue is purified by a medium pressure column chromatography with CHP-20P (eluant, water-acetonitrile). The fractions containing the desired compound are collected, and acetonitrile is distilled off under reduced pressure, and the precipitated crystals are separated by filtration to give the title compound (1.93 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05210266
Quelldatensatzuspto-grants-1993_05
ORD IDord-45fd81e8e1ef4735a88d03c53e885b71
Quellennotizuspto-grants-1993_05