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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735632Generated: November 2, 2026

tert-butyl 2-(2-(1-(bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)-2-(4-(2-hydroxyethyl)-3,5-dimethylphenyl)-N-(3-nitrobenzyl)acetamido)acetate → tert-butyl 2-(N-(3-aminobenzyl)-2-(1-(bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)-2-(4-(2-hydroxyethyl)-3,5-dimethylphenyl)acetamido)acetate

https://huagongshe.com/reaction/735632

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 2-(2-(1-(bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)-2-(4-(2-hydroxyethyl)-3,5-dimethylphenyl)-N-(3-nitrobenzyl)acetamido)acetateHCID 57842583—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-butyl 2-(N-(3-aminobenzyl)-2-(1-(bis(tert-butoxycarbonyl)amino)isoquinolin-6-ylamino)-2-(4-(2-hydroxyethyl)-3,5-dimethylphenyl)acetamido)acetateHCID 5784274691.1%

Reaction Steps

A solution of 52D (230 mg, 0.28 mmol) in MeOH (5 mL) with Pd/C (15 mg) was stirred under H2 (60 psi) for 3 h. The reaction mixture was filtered through Celite and concentrated in vacuo to afford 52E (200 mg, 90%) as a yellow solid. MS (ESI) m/z 784.85 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592331B2
Source datasetuspto-grants-2009_09
ORD IDord-eceb0aab52ed41fd85e5a395838da137
Source noteuspto-grants-2009_09