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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804625Generated: October 29, 2026

Benzyl 4-(pyrimidin-4-yl-methyl)piperazine-1-carboxylate → 4-(Piperazin-1-ylmethyl)pyrimidine

https://huagongshe.com/reaction/1804625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(pyrimidin-4-yl-methyl)piperazine-1-carboxylateHCID 67518105—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Piperazin-1-ylmethyl)pyrimidineHCID 63985039—

Reaction Steps

To 0.01 g (0.09 mmol) of 10% palladium on carbon was added a solution of 0.14 g (0.45 mmol) of the title compound from Step A in 5 mL anhydrous methanol. The resulting suspension was subjected to hydrogen at atmospheric pressure while stirring. After 4 h the mixture was filtered through a pad of Celite. The pad was washed with methanol (25 mL) and the combined filtrates were concentrated in vacuo to afford the title compound as a pale yellow residue without further purification. LC/MS: m/z (ES) 179.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354403B2
Source datasetuspto-grants-2013_01
ORD IDord-c03851bef3c544118340274da6b0aac3
Source noteuspto-grants-2013_01