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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375470Generated: November 1, 2026

Piperidine → 2,4-Dichloro-6-(piperidin-1-yl)pyrimidine

https://huagongshe.com/reaction/2375470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2,4,6-TrichloropyrimidineHCID 77378—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
Product2,4-Dichloro-6-(piperidin-1-yl)pyrimidineHCID 2110129959%

Reaction Steps

A mixture of 2,4,6-trichloropyrimidine (5.0 g, 27 mmol) and piperidine (2.3 g, 27 mmol) in tetrahydrofuran (50 mL) and N,N-diisopropylethylamine (3.5 g, 27 mmol) was stirred at room temperature for 24 hours. The solvent was removed and the crude material was purified by flash chromatography on silica gel. The column was eluted with a gradient of hexane to yield ethyl acetate/hexane (1:4). The eluent was removed, giving 2,4-dichloro-6-(1-piperidinyl)pyrimidine (3.67 g, 15.8 mmol, 59%, Rf=0.58 in ethyl acetate/hexane, 1:4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465750B2
Source datasetuspto-grants-2008_12
ORD IDord-2aa7727b12414d3a948b29e0d0269ac4
Source noteuspto-grants-2008_12