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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793723Generated: November 3, 2026

4-(3-Amino-5-methyl-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester → 4-(3,4-Diamino-5-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1793723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Amino-5-methyl-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 23541915—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product4-(3,4-Diamino-5-methyl-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 23541914—

Reaction Steps

To a stirred solution of 4-(3-Amino-5-methyl-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (15 g, 44.6 mmol) in methanol (2200 mL) was added 20% Pd(OH)2/C (1.6 g) and the suspension flushed well with nitrogen, followed by hydrogen. The resulting suspension was stirred overnight at room temperature under an atmosphere of hydrogen (ca. 1 atm). The resulting suspension was filtered under nitrogen through a pad of Celite and washed with methanol (400–500 mL). The resulting material was used immediately. LCMS (M+H)+ m/z 307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081454B2
Source datasetuspto-grants-2006_07
ORD IDord-2f0509400de4444ab9a8454d2b905f7f
Source noteuspto-grants-2006_07