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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773093Generated: November 2, 2026

3-Aminobenzenesulfonic acid → (2S)-2-amino-3-{[(3-sulfophenyl)carbamothioyl]amino}propanoic acid

https://huagongshe.com/reaction/1773093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzenesulfonic acidHCID 8474—
ReactantThiophosgeneHCID 10040—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-tert-Butyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochlorideHCID 86679032—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2S)-2-amino-3-{[(3-sulfophenyl)carbamothioyl]amino}propanoic acidHCID 866790355.5%

Reaction Steps

35 mg (0.2 mmol) of 3-aminobenzenesulfonic acid and 57 mg (0.68 mmol) of sodium hydrogen carbonate were added to a mixed solvent of 2.0 ml of water and 0.5 ml of THF, and stirred at room temperature for 15 minutes. 20 μl (0.26 mmol) of thiophosgene was added and stirred at room temperature for another 40 minutes. Subsequently, 60 mg (0.2 mmol) of tert-butyl (2S)-3-amino-2-{[(tert-butoxy)carbonyl]amino}propanoate hydrochloride was added and stirred overnight. Following extraction with ethyl acetate, the solvent was distilled away, and 4.0 ml of trifluoroacetic acid was added to the residue, and the resultant was stirred at room temperature for 5 hours. After distilling the solvent away, purification step A was used to obtain 3.5 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09253997B2
Source datasetuspto-grants-2016_02
ORD IDord-5b7b70a9e04c4ccfbdc7201446b80227
Source noteuspto-grants-2016_02