HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878477Generated: October 31, 2026
Stannane, tributyl(1-ethoxyethenyl)- → HCID 44136067, compound
https://huagongshe.com/reaction/1878477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide | HCID 44135939 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 44136067 | HCID 44136067 | 61.4% |
Reaction Steps
To a suspension of 1 g of 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in 50 mL of toluene are added 159 mg of tetrakis(triphenylphosphine)palladium and 1.09 g of tributyl(1-ethoxyvinyl)tin. The reaction mixture is heated for 9 hours at 150° C. and then for 16 hours at 130° C., and concentrated to dryness. The residue is taken up in dichloromethane and washed with aqueous 10% potassium fluoride solution. The organic phase is dried and concentrated to dryness and the residue is chromatographed on a silica cartridge, eluting with a mixture of cyclohexane and ethyl acetate. The fractions containing the expected product are combined and evaporated to dryness under reduced pressure to give 0.52 g of 6-(1-ethoxyvinyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a beige-coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314109B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-62a708f1a9db4cbc9a515bb2759635e2 |
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| Source note | uspto-grants-2012_11 |
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