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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402937Generated: October 31, 2026

Diisopropylethylamine → N5-(2-chloro-5-sulfophenyl)-L-glutamine

https://huagongshe.com/reaction/2402937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzenesulfonic acid, 4-chloro-3-nitro-, sodium salt (1:1)HCID 87246—
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—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductN5-(2-chloro-5-sulfophenyl)-L-glutamineHCID 131731744—

Reaction Steps

2 mL of methanol and 3 mL of water were added to sodium 4-chloro-3-nitrobenzensulfonate (1 mmol). 2% Pt—S/C in catalyst quantity was added thereto and stirred under hydrogen atmosphere overnight at room temperature. After filtering out the catalyst, the mixture was sufficiently dried. Then, 303 mg (1 mmol) of Boc-Glu-OtBu hydrochloride, 163 mg (1.2 mmol) of HOAt, 456 mg (1.2 mmol) of HATU, 2 mL of DMF and 0.35 mL of DIEA were added thereto and stirred at room temperature overnight. The reaction solution was diluted with water-acetonitrile and purified in accordance with the purification process A to obtain a protected form of a title compound. The obtained protected form was dissolved in 3 mL of a trifluoroacetic acid and stirred at room temperature for 2 hours. After removing a solvent, purification was conducted in accordance with the purification process A to obtain a title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796485B2
Source datasetuspto-grants-2014_08
ORD IDord-e2723213165149b2bde823a6a733d527
Source noteuspto-grants-2014_08