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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008679Generated: October 27, 2026

3,5-Dimethylpiperidine → 4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine

https://huagongshe.com/reaction/1008679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethylpiperidineHCID 118259—
Reactant4-Chloro-5-fluoro-6-(2-pentynyloxy)pyrimidineHCID 59341120—
Product4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidineHCID 5782468584.7%

Reaction Steps

0.2 g of 4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine and 0.32 g of 3,5-dimethylpiperidine (cis/trans=about 3/1) were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.23 g of 4-(3,5-dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine (hereinafter, referred to as Compound (11)). Compound (11) had the cis/trans diastereomer originated two methyls on the piperidine ring. The ratio of the cis/trans diastereomer was about 3.8/1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973028B2
Source datasetuspto-grants-2011_07
ORD IDord-916e6a2e10f4452bbeb81b31fa1b44cc
Source noteuspto-grants-2011_07