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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634646Generated: October 30, 2026

Benzyloxycarbonyl-L-phenylalanine → (2S)-6-[[(2S)-2-(benzyloxycarbonylamino)-3-phenyl-propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acid

https://huagongshe.com/reaction/1634646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonyl-L-phenylalanineHCID 70878—
Reactant(2S)-6-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 3013742—
Product(2S)-6-[[(2S)-2-(benzyloxycarbonylamino)-3-phenyl-propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 508554—

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 commercially available Nα-benzyloxycarbonyl-L-phenylalanine (300 mg, 1.2 mmol). The final product was purified by preparative HPLC to yield 33 mg (37%) of the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506786B2
Source datasetuspto-grants-2003_01
ORD IDord-0920f23fc6af4f58b93942cadb708e09
Source noteuspto-grants-2003_01