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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407960Generated: October 30, 2026

(S)-benzyl 1'-(5-ethylpyrimidin-2-yl)-2-oxo-1,4'-bipiperidin-3-ylcarbamate → (S)-3-amino-1'-(5-ethylpyrimidin-2-yl)-1,4'-bipiperidin-2-one

https://huagongshe.com/reaction/407960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-benzyl 1'-(5-ethylpyrimidin-2-yl)-2-oxo-1,4'-bipiperidin-3-ylcarbamateHCID 86688094—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(S)-3-amino-1'-(5-ethylpyrimidin-2-yl)-1,4'-bipiperidin-2-oneHCID 6747042618.6%

Reaction Steps

(S)-benzyl-1′-(5-ethylpyrimidin-2-yl)-2-oxo-[1,4′-bipiperidin]-3-ylcarbamate (2.176 g, 4.973 mmol) was dissolved in MeOH and 10% Pd/C (1 g) was added and stirred in a parr shaker at 30 psi overnight. The reaction was filtered through GF/F paper and separated on the reverse phase Horizon system to give (S)-3-amino-1′-(5-ethylpyrimidin-2-yl)-[1,4′-bipiperidin]-2-one (0.280 g, 0.9229 mmol, 18.56% yield) as a clear oil. Mass spectrum (apci) m/z=304.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-b9658f2d3aeb4e6dbea41e3597b35037
Source noteuspto-grants-2014_06