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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719101Generated: November 1, 2026

2-Aminothiophenol → N-benzyloxycarbonyl-S-(2-aminophenyl)cysteine

https://huagongshe.com/reaction/1719101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantZ-dehydro-Ala-OHHCID 4674477—
SolventEthanolHCID 702—
ProductN-benzyloxycarbonyl-S-(2-aminophenyl)cysteineHCID 5728983249.4%

Reaction Steps

23 g of α-benzyloxycarbonylaminoacrylic acid and 30 g of 2-aminobenzenethiol were dissolved in 20 ml of ethanol, and the resulting mixture was stirred at room temperature for an hour. After the solvent was distilled off, ether was added to the residue so as to cause crystallization. The precipitated crystals were separated by filtration and washed with ether to obtain 17.8 g of the desired compound. Its melting point was 150°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539151
Source datasetuspto-grants-1985_09
ORD IDord-c8d3c246ed8b402ebc4fc361dd0d0feb
Source noteuspto-grants-1985_09