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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456669Generated: October 30, 2026

((2(S)-Benzoylamino-3-methylbutyryl)-(3-nitrobenzyl)amino)acetic Acid Ethyl Ester → ((2(S)-Benzoylamino-3-methylbutyryl)-(3-aminobenzyl)amino)acetic Acid Ethyl Ester

https://huagongshe.com/reaction/1456669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant((2(S)-Benzoylamino-3-methylbutyryl)-(3-nitrobenzyl)amino)acetic Acid Ethyl EsterHCID 54107516—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product((2(S)-Benzoylamino-3-methylbutyryl)-(3-aminobenzyl)amino)acetic Acid Ethyl EsterHCID 5430789498.6%

Reaction Steps

A mixture of compound 734 (1.5 g, 3.4 mmol) and 10% Pd/C (150 mg) in MeOH (35 mL) was placed under H2 (1 atm) and stirred until the reduction was complete. The H2 was replaced with nitrogen and the reaction filtered. The filtrate was concentrated to provide 1.38 g of compound 735. ##STR114##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843904
Source datasetuspto-grants-1998_12
ORD IDord-4d90137a936e4b6291b72b8a97cb3c3f
Source noteuspto-grants-1998_12