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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431333Generated: October 30, 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/431333

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 numberUS06656965B2
Source datasetuspto-grants-2003_12
ORD IDord-16f07992e78b446c98f7049bf62e0899
Source noteuspto-grants-2003_12