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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923186Generated: November 1, 2026

Trimethylsilylacetylene → 3-((Trimethylsilyl)ethynyl)imidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/923186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromoimidazo(1,2-a)pyrazineHCID 2771671—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-((Trimethylsilyl)ethynyl)imidazo[1,2-a]pyrazineHCID 6673560291.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-bromoimidazo[1,2-a]pyrazine (0.15 g, 0.76 mmol; prepared according to J. Bradac, et al. J. Org. Chem. (1977), 42, 4197-4201), 0.09 g (0.91 mmol) of ethynyltrimethylsilane, 0.044 g (0.038 mmol) of Pd(PPh3)4, 0.014 g (0.076 mmol) of CuI, and 0.26 mL (1.52 mmol) of diisopropylethylamine in 3.8 mL of DMF was heated at 50° C. overnight under an atmosphere of N2. Upon cooling to ambient temperature, the reaction mixture was concentrated and the crude product was purified by silica gel flash chromatography (eluted with 50% EtOAc/hexanes) to provide 0.15 g of product: 216 m/z (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278971B2
Source datasetuspto-grants-2016_03
ORD IDord-38a6d98b7b764a11826560a384d856be
Source noteuspto-grants-2016_03