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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349232Generated: October 29, 2026

Dichloromethane → 2-Chloro-5-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyrimidine

https://huagongshe.com/reaction/349232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
Reactant1-But-3-ynyl-1H-[1,2,3]triazoleHCID 18453522—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product2-Chloro-5-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyrimidineHCID 86074065—

Reaction Steps

5-Bromo-2-chloro-pyrimidine (0.500 g, 2.53 mmol), 1-but-3-ynyl-1H-[1,2,3]triazole (0.368 g, 3.03 mmol) and triethyl amine (NEt3) (5.0 ml) are dissolved in DMF (10 ml) and copper iodide (CuI) (0.052 g, 0.27 mmol) is added under stirring. After passing a stream of argon through the mixture for 10 min tetrakis(triphenylphosphine)palladium(0) (0.149 g, 0.13 mmol) is added and stirring is continued for 4 h at 80° C. Dichloromethane (125 ml) is added, the mixture is washed with 0.5N hydrochloric acid (HCl) and brine, dried over Na2SO4 and concentrated in vacuo. The crude product is purified by flash column chromatography (ethyl acetate/hexanes 4:1) yielding 2-chloro-5-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyrimidine as a colorless solid. Yield 373 mg (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179812B2
Source datasetuspto-grants-2007_02
ORD IDord-f91b44a73c43430ca8b37cdd5930fb50
Source noteuspto-grants-2007_02