Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646284Generated: October 26, 2026

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

https://huagongshe.com/reaction/1646284

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-4-methylbenzoic acidHCID 75568—
Reactant2-Acetylthiomethyl-3-phenyl-propionyl chlorideHCID 10377734—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
Product3-[(2-Acetylthiomethyl-3-phenylpropionyl)amino]-4-methylbenzoic acidHCID 1567016952.4%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05179125
Source datasetuspto-grants-1993_01
ORD IDord-97369006935c489ba6952ca636ae9185
Source noteuspto-grants-1993_01