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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349237Generated: October 30, 2026

Dichloromethane → 3-Chloro-6-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyridazine

https://huagongshe.com/reaction/349237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant3-Chloro-6-iodopyridazineHCID 15418839—
Reactant1-But-3-ynyl-1H-[1,2,3]triazoleHCID 18453522—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-Chloro-6-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyridazineHCID 86074067—

Reaction Steps

3-Chloro-6-iodo-pyridazine (11.56 g, 48.1 mmol), 1-but-3-ynyl-1H-[1,2,3]triazole (6.99 g, 57.7 mmol) and triethyl amine (NEt3) (94 ml) are dissolved in DMF (188 ml) and copper iodide (CuI) (0.981 g, 5.15 mmol) is added under stirring. After passing a stream of argon through the mixture for 10 min tetrakis(triphenylphosphine)palladium(0) (2.836 g, 2.43 mmol) is added and stirring is continued for 6 h at r.t. Dichloromethane (300 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) yielding 3-chloro-6-(4-[1,2,3]triazol-1-yl-but-1-ynyl)-pyridazine as a colorless solid. Yield 9.52 g (85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179812B2
Source datasetuspto-grants-2007_02
ORD IDord-6c77992320494766b8912a493564a18b
Source noteuspto-grants-2007_02