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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092651Generated: November 4, 2026

Piperidine → 4-(2-Butynyloxy)-5-fluoro-6-piperidinopyrimidine

https://huagongshe.com/reaction/1092651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
SolventEthanolHCID 702—
Product4-(2-Butynyloxy)-5-fluoro-6-piperidinopyrimidineHCID 5934113899.2%

Reaction Steps

Into 3 ml of ethanol was resolved 0.3 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.38 g of piperidine was added therein, and the mixture was stirred for 7 hours under reflux condition. The reaction mixture was cooled to near room temperature and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.37 g of 4-(2-butynyloxy)-5-fluoro-6-piperidinopyrimidine (hereinafter, referred to as Compound (2)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129526B2
Source datasetuspto-grants-2012_03
ORD IDord-3aba55f5fa1c4f62a3890673d51ee48f
Source noteuspto-grants-2012_03