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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705445Generated: October 25, 2026

3-Amino-5-chloro-2-hydroxybenzenesulfonic acid → (2S)-2-amino-4-[(5-chloro-2-hydroxy-3-sulfophenyl)carbamoyl]butanoic acid

https://huagongshe.com/reaction/705445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5-chloro-2-hydroxybenzenesulfonic acidHCID 6927—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(4S)-5-(tert-butoxy)-4-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acidHCID 6993444—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product(2S)-2-amino-4-[(5-chloro-2-hydroxy-3-sulfophenyl)carbamoyl]butanoic acidHCID 4527568414.4%

Reaction Steps

Boc-Glu-OtBu (100 mg, 0.33 mmol) and HOBt hydrate (65.6 mg, 0.43 mmol) were dissolved in 2 mL of DMF, and triethylamine (0.137 mL) was added thereto. After cooling the mixture down to 0° C., diisopropylcarbodiimide (66.4 μL, 0.43 mmol) and 2-amino-4-chlorophenol-6-sulfonic acid (73.7 mg, 0.33 mmol) were added thereto and stirred overnight at room temperature. After removing a solvent, purification was conducted in accordance with the purification process A. The obtained intermediate was dissolved in 2 mL of TFA and stirred at room temperature for 2 hours. 2 mL of methylene chloride was added thereto, and a precipitate was taken by filtration to obtain a title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174932B2
Source datasetuspto-grants-2015_11
ORD IDord-3fbf9b2ae660433d85f427c85a84cbe1
Source noteuspto-grants-2015_11