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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330862Generated: October 26, 2026

Benzenesulfonic acid, 3-amino-5-chloro-4-methyl- → N5-(3-chloro-2-methyl-5-sulfophenyl)-L-glutamine

https://huagongshe.com/reaction/330862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 3-amino-5-chloro-4-methyl-HCID 80806—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantBoc-Glu-OtBu hydrochlorideHCID 131731743—
SolventDimethylformamideHCID 6228—
SolventTrifluoroacetic acidHCID 6422—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductN5-(3-chloro-2-methyl-5-sulfophenyl)-L-glutamineHCID 45275582—

Reaction Steps

After 2 ml of DMF and 0.52 ml (3 mmol) of DIEA were added to 303 mg (1 mmol) of Boc-Glu-OtBu hydrochloride, 221 mg (1 mmol) of 3-amino-5-chloro-4-methylbenzenesulfonic acid, 160 mg (1.3 mmol) of HOAt and 410 mg (1.3 mmol) of HATU, the mixture was stirred at room temperature overnight. The reaction solution was diluted in water-acetonitrile and purified in accordance with the purification step A to give the protected form of the product. The protected product obtained was dissolved in 5 ml of trifluoroacetic acid and stirred for 2 hours. After the solvent was removed by distillation, the mixture was purified in accordance with 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-514188b64829444189e1edd87a4f6c62
Source noteuspto-grants-2014_11