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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397787Generated: October 29, 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/397787

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-hydroxysuccimmlde 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 numberUS06610689B2
Source datasetuspto-grants-2003_08
ORD IDord-8a14b59c7209409eb115113d45598b3b
Source noteuspto-grants-2003_08