Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705031Generated: October 26, 2026

Sodium Chloride → HCID 67513398, compound

https://huagongshe.com/reaction/705031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantDiisopropylamineHCID 7912—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-(6-Bromopyridin-2-yl)pyrimidineHCID 15881258—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178479802HCID 178479802—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67513398HCID 67513398—

Reaction Conditions

Temperature50 °C

Reaction Steps

1.00 g (3.99 mmol) of 2-(6-bromopyridin-2-yl)pyrimidine, 45.5 mg (239 μmol) of copper(I) iodide and 670 μl (4.78 mmol) of N-isopropylpropane-2-amine were initially charged in 15 ml of tetrahydrofuran and degassed in an ultrasonic bath under argon. The reaction mixture was then heated to 50° C., 168 mg (239 mol) of dichloro[bis(triphenylphosphoranyl)]palladium were added and 1.70 ml (12.0 mmol) of ethynyl(trimethyl)silane were added dropwise over a period of one hour. The mixture was then stirred at 60° C. for a further two hours. For work-up, the mixture was added to semiconcentrated sodium chloride solution, the mixture was filtered through Celite and the aqueous phase was extracted repeatedly with ethyl acetate. The combined organic phases were dried over magnesium sulfate, filtered, concentrated and purified chromatographically. This gave 520 mg (51% of theory) of 2-{6-[(trimethylsilyl)ethynyl]pyridin-2-yl}pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173396B2
Source datasetuspto-grants-2015_11
ORD IDord-1298a6f452cc400ca0b63f7166fb57a9
Source noteuspto-grants-2015_11