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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403606Generated: November 1, 2026

HCID 86667974, compound → HCID 68107213, compound

https://huagongshe.com/reaction/2403606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86667974HCID 86667974—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 68107213HCID 6810721371.6%

Reaction Steps

tert-Butyl 4-(6-chloro-5-methylpyrimidin-4-yl)piperazine-1-carboxylate (400 mg) was dissolved in EtOH (8 ml), and 10% Pd/C (40 mg) was added thereto, followed by stirring at room temperature overnight under a hydrogen atmosphere. To the reaction mixture was added TEA (129 mg) and filtered using Celite as a filtration assistant, and the filtrate was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (10% to 80% EtOAc/hexane) to obtain tert-butyl 4-(5-methylpyrimidin-4-yl)piperazine-1-carboxylate (255 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-aec1564deece466da34db040b2f01abe
Source noteuspto-grants-2014_08