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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640485Generated: October 30, 2026

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

https://huagongshe.com/reaction/1640485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromoimidazo(1,2-b)pyridazineHCID 12872319—
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), Cul (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 numberUS08114874B2
Source datasetuspto-grants-2012_02
ORD IDord-dfd9f559f5ad455db8326a9995fee093
Source noteuspto-grants-2012_02