HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34100Generated: October 30, 2026
Triethylamine → HCID 68930524, compound
https://huagongshe.com/reaction/34100
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Benzodioxole, 5-ethenyl- | HCID 138986 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | HCID 68930344 | HCID 68930344 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68930524 | HCID 68930524 | 13.8% |
Reaction Steps
Under nitrogen atmosphere, 1 g of 6-fluoro-3-iodo-5-nitro-1-trityl-1H-indazole was dissolved in 10 mL of acetonitrile, added successively with 1.35 g of 5-vinyl-benzo[1,3]dioxole, 81.7 mg of palladium acetate (II), 162 mg of 2-(di-tert-butylphosphino)biphenyl and 2 mL of triethylamine, and stirred at 100° C. for 5 hours. After cooling to room temperature, 5 g of silica gel was added, and the solvent was evaporated, and purified by silica gel column chromatography, to obtain 468 mg of the crude product as yellow crystal. This crude product was washed with 50% diethylether solution in hexane, and the solvent was evaporated, to afford 143 mg of the title compound as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429609B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-af27b6d4d3c5467d8b3bbf7ae2b1d0c2 |
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| Source note | uspto-grants-2008_09 |
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