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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193348Generated: October 31, 2026

Diisopropylethylamine → tert-Butyl methyl(1-(pyrimidin-4-yl)piperidin-4-yl)carbamate

https://huagongshe.com/reaction/1193348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloropyrimidine hydrochlorideHCID 21922556—
Reactanttert-butyl N-methyl-N-(piperidin-4-ylmethyl)carbamateHCID 23004743—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Producttert-Butyl methyl(1-(pyrimidin-4-yl)piperidin-4-yl)carbamateHCID 6680551078%

Reaction Steps

tert-Butyl methyl(piperidin-4-ylmethyl)carbamate (4.67 mmol, 1.0 eq) and 4-chloropyrimidine hydrochloride (14.0 mmol, 3.0 eq) were dissolved in 2-propanol (18 ml) and DIPEA (23.33 mmol. 5.0 eq) and refluxed for 16 hours. After monitoring by TLC, the reaction solution was diluted with ethyl acetate and sat. sodium hydrogen carbonate solution, and the phases were separated. The aqueous phase was washed with ethyl acetate. The combined organic phases were washed 1× with sat. NaCl solution, dried over magnesium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, ethyl acetate:ethanol 10:1+ammonia solution). Yield: 78%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-591f2dab44124e49884ff13bf94600a1
Source noteuspto-grants-2014_03