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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093799Generated: October 26, 2026

tert-Butyl 4-(5-fluoro-6-nitro-1-oxoisoindolin-2-yl)piperidine-1-carboxylate → tert-Butyl 4-(6-amino-5-fluoro-1-oxoisoindolin-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2093799

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(5-fluoro-6-nitro-1-oxoisoindolin-2-yl)piperidine-1-carboxylateHCID 67168225—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(6-amino-5-fluoro-1-oxoisoindolin-2-yl)piperidine-1-carboxylateHCID 58257127—

Reaction Steps

The mixture of tert-butyl 4-(5-fluoro-6-nitro-1-oxoisoindolin-2-yl)piperidine-1-carboxylate (Step 3, 240 mg, 0.72 mmol), Pd (10% wt on active carbon, 24 mg) and MeOH (20 mL) was evacuated to remove air, and then the reaction was stirred under a hydrogen balloon until the starting material is consumed. Pd/C was filtered off and the solution was concentrated in vacuo to afford tert-Butyl 4-(6-amino-5-fluoro-1-oxoisoindolin-2-yl)piperidine-1-carboxylate; ESMS m/z 350.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445505B2
Source datasetuspto-grants-2013_05
ORD IDord-e6e850a3211943f98708ff735de8c234
Source noteuspto-grants-2013_05