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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431317Generated: October 30, 2026

N-tosyl-L-aspartic acid → (2S)-6-[[(2S)-4-hydroxy-4-oxo-2-(p-tolylsulfonylamino)butanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acid

https://huagongshe.com/reaction/431317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-tosyl-L-aspartic acidHCID 107597—
Reactant(2S)-6-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 3013742—
Product(2S)-6-[[(2S)-4-hydroxy-4-oxo-2-(p-tolylsulfonylamino)butanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 508564—

Reaction Steps

The title compound was prepared from solid phase bound Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-Nε-(9-fluorenylmethoxycarbonyl)-L-lysine as described in general procedure Bb using Nα-(4-methylbenzenesulfonyl)-L-aspartic acid (340 mg, 1.2 mmol) prepared in step A of this example. The final product was purified by preparative HPLC to yield 20 mg (26%) of the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656965B2
Source datasetuspto-grants-2003_12
ORD IDord-92ddc191653743f2bc02d32163cbece6
Source noteuspto-grants-2003_12