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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557722Generated: October 30, 2026

4-(5-Nitro-pyrimidin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester → 1,1-Dimethylethyl 4-(5-amino-2-pyrimidinyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/557722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Nitro-pyrimidin-2-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 66738557—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 4-(5-amino-2-pyrimidinyl)-1-piperazinecarboxylateHCID 59464319—

Reaction Steps

To a solution of 4-(5-nitro-pyrimidin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester (927 mg, 3 mmol, prepared from 2-chloro-5-nitropyrimidine and N-Boc-piperazine) in tetrahydrofuran (20 mL) and methanol (30 mL) was added 10% palladium on carbon (240 mg) and the mixture was hydrogenated at 50 psi for 1 hr. The mixture was filtered and the solvents were evaporated. The residue was dried in vacuum to give 4-(5-amino-pyrimidin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058299B2
Source datasetuspto-grants-2011_11
ORD IDord-6702fb79851248e9a2eb4117e62ca430
Source noteuspto-grants-2011_11