HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422491Generated: October 27, 2026
Potassium Carbonate → 6-Fluoro-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine
https://huagongshe.com/reaction/422491
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-5-fluoropyridine | HCID 2737701 | — |
| Reactant | 1-Bromo-6-(trimethylsilyl)hex-5-yn-2-one | HCID 86086769 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Fluoro-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine | HCID 66597925 | 30.4% |
Reaction Steps
To a stirred solution of 1-bromo-6-(trimethylsilyl)hex-5-yn-2-one (2.50 g, 10.11 mmol) in EtOH (8 mL) was added potassium carbonate (350 mg, 2.53 mmol) and 5-fluoropyridin-2-amine (567 mg, 5.06 mmol). The mixture was heated at 80° C. overnight. The mixture was concentrated, the residue was dissolved in EtOAc, and the organic layer was washed with brine, dried over MgSO4 filtered and concentrated under reduced pressure. The crude residue was purified over silicagel chromatography (prepacked 70 g silicagel column, from DCM/MeOH: 100/0 to 96/4 as eluent) to afford 400 mg of 6-fluoro-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine (Yield: 30%) as an orange-brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101637B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-a95faf1b073343f7a728dbaac1f20ae3 |
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| Source note | uspto-grants-2012_01 |
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