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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490448Generated: October 25, 2026

Potassium Fluoride → 5-Chloro-3-ethynylpyridin-2-amine

https://huagongshe.com/reaction/490448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant5-Chloro-3-((trimethylsilyl)ethynyl)pyridin-2-amineHCID 24729465—
SolventMethanolHCID 887—
Product5-Chloro-3-ethynylpyridin-2-amineHCID 2591866789.3%

Reaction Steps

A suspension of 1.6 g of 5-chloro-3-trimethylsilanylethynylpyridin-2-ylamine and 1.24 g of potassium fluoride in 80 ml of methanol is brought to reflux for approximately 3 hours 30 minutes. After returning to a temperature in the region of 20° C., the mixture is filtered through celite, and the insoluble material is washed three times with 50 ml of methanol. The filtrate is concentrated to dryness under reduced pressure (13 kPa). The residue is taken up with 100 ml of dichloromethane. The solution obtained is washed with three times 60 ml of water, dried over magnesium sulfate, filtered, and concentrated to dryness under reduced pressure (13 kPa). 0.97 g of 5-chloro-3-ethynylpyridin-2-ylamine is thus obtained in the form of a solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528147B2
Source datasetuspto-grants-2009_05
ORD IDord-fbb17af726ac46589fe669405f1ad55a
Source noteuspto-grants-2009_05