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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397804Generated: October 28, 2026

Nalpha-isobutyl-Nalpha-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride → (2S)-2-[(4-aminophenyl)sulfonyl-isobutyl-amino]-6-[[(2S)-2-[[2-(4-methoxyphenyl)acetyl]amino]-3-phenyl-propanoyl]amino]hexanoic acid

https://huagongshe.com/reaction/397804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNalpha-isobutyl-Nalpha-(4-nitrobenzenesulfonyl)-L-lysine hydrochlorideHCID 69107784—
ReactantNalpha-(4-methoxyphenylacetyl)-L-phenylalanineHCID 69347446—
Product(2S)-2-[(4-aminophenyl)sulfonyl-isobutyl-amino]-6-[[(2S)-2-[[2-(4-methoxyphenyl)acetyl]amino]-3-phenyl-propanoyl]amino]hexanoic acidHCID 508685—

Reaction Steps

The title compound was prepared from Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-L-lysine hydrochloride (200 mg, 0.45 mmol, example 5, step C) as described in general procedure Bc using Nα-(4-methoxyphenylacetyl)-L-phenylalanine (example 132, step A). The final product, Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-Nε-[N′α-(4-methoxyphenylacetyl)-L-phenylalanyl]-L-lysine was subsequently hydrogenolysed following the indications of general procedure E. Purification by HPLC gave the desired material (7 mg, 4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610689B2
Source datasetuspto-grants-2003_08
ORD IDord-6244e887648244baa5ae59401c3274be
Source noteuspto-grants-2003_08