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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18934Generated: October 25, 2026

4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one → 4-(4-amino-2-tert-butyl-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one

https://huagongshe.com/reaction/18934

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 58679272—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(4-amino-2-tert-butyl-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 5867925993%

Reaction Steps

A mixture of the previously prepared 4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one (80 mg, 0.25 mmol) dissolved in methanol (2 mL) and Pd on charcoal (10% w/w, 20 mg) was shaken under hydrogen atmosphere in a Parr shaker at 50 psi for 18 hours. The reaction was filtered through celite, the residue concentrated under vacuum to afford 68 mg of the desired 4-(4-amino-2-tert-butyl-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741479B2
Source datasetuspto-grants-2010_06
ORD IDord-aeba203d1bc24ab79b8a60a2fe020729
Source noteuspto-grants-2010_06