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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839506Generated: November 2, 2026

L-Tryptophan, N-[(4-methylphenyl)sulfonyl]- → methyl (2S)-6-[[(2S)-3-(1H-indol-3-yl)-2-(p-tolylsulfonylamino)propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoate

https://huagongshe.com/reaction/1839506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Tryptophan, N-[(4-methylphenyl)sulfonyl]-HCID 1190064—
ReactantNalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-L-lysine methyl esterHCID 22975548—
SolventHydrochloric AcidHCID 313—
Solventpotassium carbonate THFHCID 86626146—
Productmethyl (2S)-6-[[(2S)-3-(1H-indol-3-yl)-2-(p-tolylsulfonylamino)propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoateHCID 50859271%

Reaction Steps

To a stirred solution of Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-L-lysine methyl ester (369 mg, 1 mmol, example 65, step C) in THF/K2CO3 (1M) (3 mL/3 mL) was added Nα-(4-methylbenzenesulfonyl)-L-tryptophan N-hydroxysuccininide ester (547 mg, 1.2 mmol). The reaction mixture was stirred overnight, then diluted with 1N HCl and extracted with EtOAc. The organic layer was dried (MgSO4) and concentrated. The crude was purified by flash chromatography using hexane/EtOAc as eluent to afford the desired product (71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677367B2
Source datasetuspto-grants-2004_01
ORD IDord-fb38dc784ff04159a8e70a23c72f01b7
Source noteuspto-grants-2004_01