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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020048Generated: October 31, 2026

HCID 59508997, compound → HCID 59509002, compound

https://huagongshe.com/reaction/1020048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59508997HCID 59508997—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59509002HCID 5950900287.8%

Reaction Steps

4-[6-(2-Fluoro-6-methoxy-phenyl)-pyrimidin-4-ylcarbamoyl]-piperidine-1-carboxylic acid benzyl ester (XXIII) (0.05 g, 0.1 mmol) was dissolved in methanol (5 ml) and 10% Pd/C (0.03 g) was added under an atmosphere of nitrogen. The mixture 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. The resulting crude product was triturated with dry diethyl ether (2 ml) and concentrated to yield piperidine-4-carboxylic acid [6-(2-fluoro-6-methoxy-phenyl)-pyrimidin-4-yl]-amide (compound #12A) (0.029 g, 81%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716296B2
Source datasetuspto-grants-2014_05
ORD IDord-e291aa1987ce4d76b55e6fa4076267ea
Source noteuspto-grants-2014_05