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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397763Generated: October 29, 2026

(2S)-3-Hydroxy-2-(4-methylbenzenesulfonamido)propanoic acid → (2S)-6-[[(2S)-3-hydroxy-2-(p-tolylsulfonylamino)propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acid

https://huagongshe.com/reaction/397763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-3-Hydroxy-2-(4-methylbenzenesulfonamido)propanoic acidHCID 774825—
Reactant(2S)-6-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 3013742—
Product(2S)-6-[[(2S)-3-hydroxy-2-(p-tolylsulfonylamino)propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 508555—

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-serine (150 mg, 1.2 mmol) prepared in step A of this example. The final product was purified by preparative HPLC to yield 35 mg (46%) of the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610689B2
Source datasetuspto-grants-2003_08
ORD IDord-40318b0b321442c2bf1dacb49a42a0c4
Source noteuspto-grants-2003_08