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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020036Generated: October 26, 2026

4-[6-(2-Methoxy-phenyl)-pyrimidin-4-ylcarbamoyl]-piperidine-1-carboxylic acid benzyl ester → Piperidine-4-carboxylic acid [6-(2-methoxy-phenyl)-pyrimidin-4-yl]amide

https://huagongshe.com/reaction/1020036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[6-(2-Methoxy-phenyl)-pyrimidin-4-ylcarbamoyl]-piperidine-1-carboxylic acid benzyl esterHCID 59509094—
CatalystPalladiumHCID 23938—
SolventDichloromethane methanolHCID 21226129—
ProductPiperidine-4-carboxylic acid [6-(2-methoxy-phenyl)-pyrimidin-4-yl]amideHCID 5950894660.8%

Reaction Steps

4-[6-(2-Methoxy-phenyl)-pyrimidin-4-ylcarbamoyl]-piperidine-1-carboxylic acid benzyl ester (XI) (0.45 g, 1.00 mmol) was dissolved in methanol:dichloromethane (4:1) (24 ml) and 10% Pd/C (0.2 g) was added under an atmosphere of nitrogen. The reaction was stirred at room temperature under hydrogen balloon pressure for 18 hours. The catalyst was removed from the reaction mixture by filtration through a celite bed and the filtrate was evaporated to dryness. Then the crude product was treated with dry diethyl ether (10 ml) and the solid was filtered to obtain piperidine-4-carboxylic acid [6-(2-methoxy-phenyl)-pyrimidin-4-yl]-amide (compound #6A) (0.19 g, 42%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716296B2
Source datasetuspto-grants-2014_05
ORD IDord-49108ffaf7b4474086a61cc9b9a02486
Source noteuspto-grants-2014_05