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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804620Generated: October 30, 2026

Benzyl 4-(2-(benzyloxy)pyridin-3-yl)piperazine-1-carboxylate → 3-piperazin-1-ylpyridin-2(1H)-one

https://huagongshe.com/reaction/1804620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(2-(benzyloxy)pyridin-3-yl)piperazine-1-carboxylateHCID 67060675—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-piperazin-1-ylpyridin-2(1H)-oneHCID 6797206688%

Reaction Steps

To a 10 mL round bottomed flask was added 10 mg (0.009 mmol) of 10% palladium on activated carbon which was then flushed with nitrogen. Next, a solution of 0.090 (0.22 mmol) of benzyl 4-[2-(benzyloxy)pyridin-3-yl]piperazine-1-carboxylate from Step A above in 4 mL of methanol was added and the resulting mixture was placed under an atmosphere of hydrogen gas at atmospheric pressure for 3 h. The reaction was then flushed with nitrogen and filtered through a pad of Celite®. The pad was washed with methanol and the combined organics were evaporated to dryness to afford the title compound as a clear gum (0.035 g, 88%). LC-MS: m/z (ES) 180.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354403B2
Source datasetuspto-grants-2013_01
ORD IDord-c2f15bd675e64faf960ff61965aa5eb8
Source noteuspto-grants-2013_01