HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363752Generated: October 29, 2026
Trimethylsilylacetylene → Ethyl 6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]pyridine-2-carboxylate
https://huagongshe.com/reaction/2363752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Ethyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylate | HCID 3681971 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | Ethyl 6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]pyridine-2-carboxylate | HCID 44136341 | — |
Reaction Steps
A mixture of 4 g of ethyl 6-iodoimidazo[1,2-a]pyridine-2-carboxylate, 2.63 mL of ethynyltrimethylsilane and 888 mg of dichlorobis(triphenylphosphine)palladium is degassed under vacuum. 240 mg of degassed N,N-dimethylformamide and 3.52 mL of triethylamine are added. The reaction mixture is degassed under argon, stirred at 50° C. for 50 hours and then cooled and diluted with 20 mL of water. The precipitate is filtered off by suction and washed with 5 mL of water and then chromatographed on silica, eluting with mixtures of ethyl acetate and hexane (from 50/50 to 90/10). The fractions containing the expected product are combined and concentrated to dryness under reduced pressure to give 3.6 g of ethyl 6-[(trimethylsilyl)ethynyl]imidazo[1,2-a]pyridine-2-carboxylate in the form of an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691990B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-ca67b75e54e749fc82854ca95a158990 |
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| Source note | uspto-grants-2014_04 |
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