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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993635Generated: October 30, 2026

Methanol → 1-Boc-4-(5-amino-6-methyl-2-pyridinyl)piperazine

https://huagongshe.com/reaction/1993635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Boc-4-(6-methyl-5-nitro-2-pyridinyl)-piperazineHCID 68538037—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-4-(5-amino-6-methyl-2-pyridinyl)piperazineHCID 5913445199%

Reaction Steps

Mix a slurry of 4-(6-methyl-5-nitro-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester (46.00 g, 142.7 mmol) in THF (750 mL) at room temperature with Pd/C (5% Aldrich, 3.04 g, 1.43 mmol) then place under a hydrogen atmosphere (Parr shaker, 40-45 psi) for 6 hours. Add MeOH (250 mL), and subject the slurry to an atmosphere of hydrogen for 4 hours at room temperature. Add additional catalyst (3.04 g), then place the mixture under hydrogen for 7 hours. Filter the mixture through a pad of Celite 521®, washing with THF and MeOH then concentrate under reduced pressure to provide the title compound a pale pink solid. (41.58 g, 99% yield, MS(ES+): m/z=293 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652015B2
Source datasetuspto-grants-2010_01
ORD IDord-c34a8db5a40047efbbf4d91a17a0178e
Source noteuspto-grants-2010_01