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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571316Generated: November 1, 2026

HCID 86681725, compound → HCID 86681724, compound

https://huagongshe.com/reaction/571316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86681725HCID 86681725—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86681724HCID 8668172498%

Reaction Steps

A mixture of benzyl 2-(5-(N-(2-(tert-butoxycarbonyl(2-methoxyethyl)-amino)ethyl)methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (0.166 g, 0.282 mmol) and 10% w/w Pd/C (a catalytic amount) in MeOH was hydrogenated in a Parr apparatus at 30 psi for 3 hours. The catalyst was filtered off and the filtrate was evaporated to dryness affording 2-(5-(N-(2-(tert-butoxycarbonyl(2-methoxyethyl)amino)ethyl)-methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetic acid (0.138 g, 0.276 mmol, 98% yield, MS/ESI+ 522.0 [MNa]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-3613554ebf0d4ea498b69fb96fabb3e2
Source noteuspto-grants-2015_05