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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020038Generated: October 27, 2026

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

https://huagongshe.com/reaction/1020038

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[6-(2-Isopropoxy-phenyl)-pyrimidin-4-ylcarbamoyl]-piperidine-1-carboxylic acid benzyl esterHCID 59509086—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductPiperidine-4-carboxylic acid [6-(2-isopropoxy-phenyl)-pyrimidin-4-yl]-amideHCID 5950900952.6%

Reaction Steps

4-[6-(2-lsopropoxy-phenyl)-pyrimidin-4-ylcarbamoyl]-piperidine-1-carboxylic acid benzyl ester (XIII) (0.32 g, 0.67 mmol) was dissolved in methanol (20 ml) and 10% Pd/C (0.17 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 reaction mixture by filtration through a celite bed and the filtrate was evaporated to dryness. Then the crude product was triturated with dry diethyl ether (10 mL) and the resulting solid was filtered to obtain piperidine-4-carboxylic acid [6-(2-isopropoxy-phenyl)-pyrimidin-4-yl]-amide (compound #7A) (0.12 g, 52%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716296B2
Source datasetuspto-grants-2014_05
ORD IDord-286ab5dd8b5c4d8a91bfd5b2afdc8f84
Source noteuspto-grants-2014_05