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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431332Generated: October 30, 2026

N-((4-Methylphenyl)sulfonyl)-L-phenylalanine → methyl (2S)-2-[isobutyl(p-tolylsulfonyl)amino]-6-[[(2S)-3-phenyl-2-(p-tolylsulfonylamino)propanoyl]amino]hexanoate

https://huagongshe.com/reaction/431332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-((4-Methylphenyl)sulfonyl)-L-phenylalanineHCID 99327—
ReactantNalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-L-lysine methyl esterHCID 22975548—
SolventHydrochloric AcidHCID 313—
Solventpotassium carbonate THFHCID 86626146—
Productmethyl (2S)-2-[isobutyl(p-tolylsulfonyl)amino]-6-[[(2S)-3-phenyl-2-(p-tolylsulfonylamino)propanoyl]amino]hexanoateHCID 50859177%

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-phenylalanine N-hydroxysuccinimmide ester (500 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 (77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656965B2
Source datasetuspto-grants-2003_12
ORD IDord-37e2149c61e044ad96134a1cf2122458
Source noteuspto-grants-2003_12