Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839505Generated: November 3, 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/1839505

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 numberUS06677367B2
Source datasetuspto-grants-2004_01
ORD IDord-7ab23cc5125844b1a1a7ff641d27b7ce
Source noteuspto-grants-2004_01