HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360700Generated: November 1, 2026
Stannane, tributyl(1-ethoxyethenyl)- → HCID 16065044, compound
https://huagongshe.com/reaction/1360700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | HCID 16065043 | HCID 16065043 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16065044 | HCID 16065044 | — |
Reaction Steps
To a solution of 1-(4-bromo-2,6-difluorophenyl)-6-(2,4-difluorophenyl)-2H-quinolizin-2-one (30 mg, 0.067 mmol) in toluene (1.4 mL) was added tributyl(1-ethoxyvinyl)stannane and tetrakis(triphenylphosphine)palladium (7.74 mg, 0.007 mmol) and heated to 90° C. for 1½ h. The reaction was cooled, filtered through celite, and diluted with THF. The mixture was added 2N HCl and stirred for 20 min to complete the reaction. The crude mixture was diluted with H2O and EtOAc. The organic layer was washed with H2O, brine, dried over MgSO4, and condensed. The crude residue was purified via silica gel chromatography (hexanes/ethyl acetate) to give the title compound (7.9 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879875B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-df881b32556a405586587685ca113cfe |
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| Source note | uspto-grants-2011_02 |
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