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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Bromoimidazo(1,2-a)pyrazine | HCID 2771671 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-((Trimethylsilyl)ethynyl)imidazo[1,2-a]pyrazine | HCID 66735602 | 91.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278971B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-38a6d98b7b764a11826560a384d856be |
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| Source note | uspto-grants-2016_03 |
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