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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330855Generated: October 25, 2026

3-Amino-5-chloro-2-hydroxybenzenesulfonic acid → N5-(2-hydroxy-3-sulfophenyl)-L-glutamine

https://huagongshe.com/reaction/330855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5-chloro-2-hydroxybenzenesulfonic acidHCID 6927—
ReactantTetrahydrofuranHCID 8028—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(4S)-5-(Benzyloxy)-4-(((benzyloxy)carbonyl)amino)-5-oxopentanoic acidHCID 6994031—
SolventDichloromethaneHCID 6344—
ProductN5-(2-hydroxy-3-sulfophenyl)-L-glutamineHCID 12393741940%

Reaction Steps

Z-Glu-OBn (371 mg, 1 mmol) was dissolved in methylene chloride (1 ml), and CDI (180 mg, 1.1 mmol) was added to the solution. The mixture was stirred at room temperature for 30 minutes. 2-Amino-4-chlorophenol-6-sulfonic acid (223 mg, 1 mmol) and THF (1 ml) were added to the mixture. The mixture was then stirred overnight at room temperature. After the solvent was removed by distillation, the mixture was purified in accordance with the purification step A. The resulting intermediate was dissolved in a methanol-water solvent mixture. A catalytic amount of Pd/C was added to the solution. The mixture was stirred overnight at room temperature in a hydrogen atmosphere. After the catalyst was filtered off, the solvent was removed by distillation. The mixture was purified according to the purification step A to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877739B2
Source datasetuspto-grants-2014_11
ORD IDord-03ebc8ca46bf4cd7a829e4f089ea504c
Source noteuspto-grants-2014_11