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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839483Generated: November 3, 2026

Nalpha(4-nitrobenzenesulfonyl)-L-tryptophan → (2S)-6-[[(2S)-3-(1H-indol-3-yl)-2-[(4-nitrophenyl)sulfonylamino]propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acid

https://huagongshe.com/reaction/1839483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNalpha(4-nitrobenzenesulfonyl)-L-tryptophanHCID 1572095—
ReactantNalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-L-lysineHCID 23552860—
Product(2S)-6-[[(2S)-3-(1H-indol-3-yl)-2-[(4-nitrophenyl)sulfonylamino]propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 508531—

Reaction Steps

The title compound was prepared from Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-L-lysine (100 mg, 0.29 mmol, example 1, step E) as described in general procedure Bc using Nα-(4-nitrobenzenesulfonyl)-L-tryptophan (120 mg, 0.3 mmol) which was prepared in step A of example 5. The final product was purified by HPLC to give 66 mg (36%) of pure adduct.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677367B2
Source datasetuspto-grants-2004_01
ORD IDord-49ff2b22e8d14b56884d45451959369c
Source noteuspto-grants-2004_01