HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746831Generated: October 31, 2026
3-Aminobenzenesulfonic acid → (2S)-2-amino-3-{[(3-sulfophenyl)carbamothioyl]amino}propanoic acid
https://huagongshe.com/reaction/1746831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminobenzenesulfonic acid | HCID 8474 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (S)-tert-Butyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochloride | HCID 86679032 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S)-2-amino-3-{[(3-sulfophenyl)carbamothioyl]amino}propanoic acid | HCID 86679035 | 5.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150505B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-bb6cd2f7438946de8351c5756f7cb2ed |
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| Source note | uspto-grants-2015_10 |
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