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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468308Generated: 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/1468308

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 Conditions

Temperature0 °C

Reaction Steps

Boc-Glu-OtBu (100 mg, 0.33 mmol) and HOBt monohydrate (65.6 mg, 0.43 mmol) were dissolved in 2 ml of DMF, and triethylamine (0.137 ml) was added to the solution. After cooling 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, followed by stirring at room temperature overnight. After the solvent was removed by distillation, the mixture was purified according to the purification step A. The resulting intermediate was dissolved in 2 ml of TFA. The solution was stirred at room temperature for 2 hours, and 2 ml of methylene chloride was added thereto. The precipitate was taken out by filtration to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000208B2
Source datasetuspto-grants-2015_04
ORD IDord-b2638b7403f545889f8628281a49af40
Source noteuspto-grants-2015_04