HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468295Generated: November 1, 2026
2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 86710110, compound
https://huagongshe.com/reaction/1468295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5233012 | — |
| Reactant | HCID 86710111 | HCID 86710111 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86710110 | HCID 86710110 | 70% |
Reaction Steps
3-(4,4-Difluorocyclohexylmethyl)-6-iodo-2-trifluoromethylimidazo[1,2-a]pyridine-7-carbonitrile (20.0 mg, 0.0430 mmol) obtained in step 2 was dissolved in 1,2-dichloromethane (0.60 mL), and the solution was stirred at 60° C. for 1 hour after adding 4,4,5,5-tetramethyl-2-vinyl-1,3,2-dioxaborolane (24.0 mg, 0.153 mmol), tetrakis(triphenylphosphine)palladium(0) (4.93 mg, 0.00426 mmol), and water (0.2 mL). The reaction mixture was filtered through Celite (registered trademark), and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=90/10→50/50) to give 3-(4,4-difluorocyclohexylmethyl)-2-trifluoromethyl-6-vinylimidazo[1,2-a]pyridine-7-carbonitrile (11.0 mg, yield 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000186B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-c4cd555fe1364e89be0fb9566ff65646 |
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| Source note | uspto-grants-2015_04 |
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