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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958094Generated: November 3, 2026

tert-Butyl 4-((4-nitrobenzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylate → tert-Butyl 4-((4-aminobenzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1958094

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-((4-nitrobenzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylateHCID 59302730—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-((4-aminobenzo[d]oxazol-2-yl)methyl)piperazine-1-carboxylateHCID 5930272691%

Reaction Steps

To a solution of tert-butyl 4((4-nitrobenzo[d]oxazol-2-yl)methyl)-piperazine-1-carboxylate (5.97 g, 16.6 mmol, 1.0 equiv) in MeOH (49 mL) was added Pd/C (10% Pd, wet, 2.99 g). The resulting suspension was fixed with a hydrogen balloon and sparged with hydrogen while stirring was maintained. After 1 h, the mixture was filtered through a pad of celite and concentrated in vacuo to provide the title compound as an off-white solid (5.0 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410108B2
Source datasetuspto-grants-2013_04
ORD IDord-91b22a2a7ce147d899157e6381913c69
Source noteuspto-grants-2013_04