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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193344Generated: October 30, 2026

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

https://huagongshe.com/reaction/1193344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloropyridineHCID 12288—
ReactantDiisopropylethylamineHCID 81531—
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)methyl)carbamateHCID 6680533651%

Reaction Steps

tert-Butyl methyl(piperidin-4-ylmethyl)carbamate (1.4 mmol, 1.0 eq) and 4-chloropyridine (4.2 mmol, 3.0 eq) were dissolved in 2-propanol (5 ml) and DIPEA (7.0 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 dried over magnesium sulfate, concentrated under reduced pressure and purified by column chromatography (silica gel, ethyl acetate:ethanol 10:1+ammonia solution). Yield: 51%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-bb171c432a9b41bb922c24e5ec84f199
Source noteuspto-grants-2014_03