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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622531Generated: October 27, 2026

Trimethylsilylacetylene → 3-((Trimethylsilyl)ethynyl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1622531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromoimidazo(1,2-b)pyridazineHCID 12872319—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-((Trimethylsilyl)ethynyl)imidazo[1,2-b]pyridazineHCID 6673556971.1%

Reaction Steps

A mixture of 3-bromoimidazo[1,2-b]pyridazine (36.78 g, 0.186 mol; prepared according to Stanovnik, B. et al. Synthesis (1981), 12, 987-989), ethynyltrimethylsilane (21.89 g, 0.223 mol), Pd(PPh3)4 (10.73 g, 9.29 mmol), CuI (5.30 g, 0.028 mol), and diisopropylethylamine (32.4 mL, 0.279 mol) in 150 mL of DMF was stirred at ambient temperature, under an atmosphere of N2, for 1 h. The reaction mixture was concentrated and the crude product was purified by silica gel flash chromatography (eluted with 0-5% MeOH/DCM) to provide 28.46 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778942B2
Source datasetuspto-grants-2014_07
ORD IDord-f7dc8ee532b743a3a0d26fd737428600
Source noteuspto-grants-2014_07