HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902025Generated: October 31, 2026
Triphenylphosphine → HCID 59700621, compound
https://huagongshe.com/reaction/902025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 69221493 | HCID 69221493 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59700621 | HCID 59700621 | 130.4% |
Reaction Steps
Combine 7-bromo-4-[2-(6-methyl-pyridin-2-yl)-pyrazolo[1,5-a]pyridin-3-yl]-quinoline (0.18 g, 0.43 mmol), triphenylphosphine (36 mg, 0.14 mmol), sodium acetate (0.05 g, 0.61 mmol), methanol (2.7 mL), and DMF (2.7 mL). Bubble nitrogen gas through the solution for 10 minutes. Add palladium acetate (0.03 g, 0.13 mmol). Bubble nitrogen gas through the solution for another 10 minutes. Connect a carbon monoxide balloon to the reaction vessel and heat at 80° C. for 24 hours. Evaporate the solvent in vacuo. Chromatograph the residue on silica gel (elute with 50% ethyl acetate/hexanes then 75% ethyl acetate/hexanes) to afford the title compound 72 mg (42%) as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365066B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-1042b126e0784c9b9eeea843866ce9c8 |
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| Source note | uspto-grants-2008_04 |
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