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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248704Generated: October 27, 2026

Hydrochloric Acid → Ethyl 3-[(2-mercaptomethyl-3-phenylpropionyl)amino]benzoate

https://huagongshe.com/reaction/248704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyrrolidineHCID 31268—
ReactantEthyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)amino]benzoateHCID 15670143—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-[(2-mercaptomethyl-3-phenylpropionyl)amino]benzoateHCID 1567025128.1%

Reaction Steps

Ethyl 3-[(2-acetylthiomethyl-3-phenylpropionyl)-amino]benzoate (compound of Example 68-(a)-[1]) (2.0 g) is dissolved in a 80% aqueous acetonitrile, and thereto is added pyrrolidine (0.5 g), and the mixture is stirred at room temperature for 30 minutes. The mixture is adjusted to pH 5.0 with 10% hydrochloric acid, and acetonitrile is distilled off under reduced pressure, and the residue is extracted with ethyl acetate (50 ml). The extract is washed with water, and ethyl acetate is distilled off under reduced pressure. The 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. The aqueous solution is extracted with ethyl acetate (50 ml), and the extract is dried over anhydrous magnesium sulfate, and ethyl acetate is distilled off under reduced pressure to give the title compound (0.5 g) as an oily substance. IR (film; cm-1): 1710, 1660 Elementary analysis for C19H21NO3S: Calcd. (%): C,66.45; H,6.16; N,4.08; S,9.34 Found (%): C,66.37; H,6.25; N,4.04; S,9.05

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210266
Source datasetuspto-grants-1993_05
ORD IDord-24d07538e90243bcab697813f004f33e
Source noteuspto-grants-1993_05