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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397761Generated: October 29, 2026

N-(2-Thienylsulfonyl)-L-phenylalanine → (2S)-2-[isobutyl-(4-nitrophenyl)sulfonyl-amino]-6-[[(2S)-3-phenyl-2-(2-thienylsulfonylamino)propanoyl]amino]hexanoic acid

https://huagongshe.com/reaction/397761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Thienylsulfonyl)-L-phenylalanineHCID 704092—
Reactant(2S)-6-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[isobutyl-(4-nitrophenyl)sulfonyl-amino]hexanoic acidHCID 3013754—
Product(2S)-2-[isobutyl-(4-nitrophenyl)sulfonyl-amino]-6-[[(2S)-3-phenyl-2-(2-thienylsulfonylamino)propanoyl]amino]hexanoic acidHCID 508552—

Reaction Steps

The title compound was prepared from solid phase bound Nα-isobutyl-Nα-(4-nitrobenzenesulfonyl)-Nε-(9-fluorenylmethoxycarbonyl)-L-lysine as described in general procedure Bb using Nα-(2-thiophenesulfonyl)-L-phenylalanine (300 mg, 1.2 mmol) which was prepared in step A of example 24. The final product was purified by preparative HPLC to yield 46 mg (54%) of the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610689B2
Source datasetuspto-grants-2003_08
ORD IDord-13191d004f4c440c9fecf17061ea58b1
Source noteuspto-grants-2003_08