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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431339Generated: October 25, 2026

O-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosine → (2S)-6-[[(2S)-3-(4-benzyloxyphenyl)-2-(tert-butoxycarbonylamino)propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acid

https://huagongshe.com/reaction/431339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosineHCID 98763—
ReactantNalpha-isobutyl-Nalpha-(4-methylbenzenesulfonyl)-L-lysineHCID 23552860—
Product(2S)-6-[[(2S)-3-(4-benzyloxyphenyl)-2-(tert-butoxycarbonylamino)propanoyl]amino]-2-[isobutyl(p-tolylsulfonyl)amino]hexanoic acidHCID 508608—

Reaction Steps

The title compound was prepared from Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-L-lysine (100 mg, 0.29 mmol, example 1, step E) as described in general procedure Bc using commercially available Nα-tert-butoxycarbonyl-O-benzyl-L-tyrosine (111 mg, 0.3 mnol). The final product was triturated with ether to yield 145 mg (68%) of the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656965B2
Source datasetuspto-grants-2003_12
ORD IDord-241bf21b3dba4af88b1214533b5932cf
Source noteuspto-grants-2003_12