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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193416Generated: November 1, 2026

Benzyl 1-(2,6-dimethylpyrimidin-4-yl)piperidin-4-yl(ethyl)carbamate → 1-(2,6-dimethylpyrimidin-4-yl)-N-ethylpiperidin-4-amine

https://huagongshe.com/reaction/1193416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 1-(2,6-dimethylpyrimidin-4-yl)piperidin-4-yl(ethyl)carbamateHCID 66798660—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product1-(2,6-dimethylpyrimidin-4-yl)-N-ethylpiperidin-4-amineHCID 5493953766%

Reaction Steps

A solution of benzyl 1-(2,6-dimethylpyrimidin-4-yl)piperidin-4-yl(ethyl)carbamate (960 mg, 2.6 mmol, 1.0 eq) in MeOH (40 ml) was degassed for 15 minutes with nitrogen; Pd(OH)2 (480 mg) was added and hydrogenation was carried out for 1 hour at RT. After monitoring by TLC, the reaction mixture was filtered off over Celite and washed with MeOH (100 ml) and the filtrate was concentrated under reduced pressure and dried. Yield: 66% (400 mg, 1.709 mmol) C. Single Substance Syntheses General Method for the Synthesis of the Illustrative Compounds (H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-fc0f9ce8d7e04ed6847afb6e758a56eb
Source noteuspto-grants-2014_03