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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14513Generated: October 24, 2026

2-Methylpiperidine → 4-(2-Butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine

https://huagongshe.com/en/reaction/14513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpiperidineHCID 7974—
Reactant4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
SolventEthanolHCID 702—
Product4-(2-Butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidineHCID 5934111571.1%

Reaction Steps

Into 3 ml of ethanol was resolved 0.3 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.45 g of 2-methylpyperidine was added therein, and the mixture was stirred for 5 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 0.28 g of 4-(2-butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine (hereinafter, referred to as Compound (1)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732448B2
Source datasetuspto-grants-2010_06
ORD IDord-128a683dc56a4a128028ba8b3f713edc
Source noteuspto-grants-2010_06