HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34047Generated: October 26, 2026
3-Bromopyridine → 4-Methoxy-3-[(E)-2-(pyridin-3-yl)-vinyl]-1-trityl-1H-indazole-5-carbonitrile
https://huagongshe.com/reaction/34047
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Phosphine, tris(4-methylphenyl)- | HCID 13956 | — |
| Reactant | 3-vinyl-4-methoxy-1-trityl-1H-indazole-5-carbonitrile | HCID 23070127 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Methoxy-3-[(E)-2-(pyridin-3-yl)-vinyl]-1-trityl-1H-indazole-5-carbonitrile | HCID 68928542 | — |
Reaction Steps
300 mg of 3-vinyl-4-methoxy-1-trityl-1H-indazole-5-carbonitrile and 180 μl of 3-bromopyridine were dissolved in a mixed solvent of 1 mL triethylamine/5 mL acetonitrile, added with 40 mg of tri-p-tolylphosphine and 27 mg of palladium acetate (II), and heated at 110° C. for 24 hours. The reaction solution was added with silica gel, the solvent was evaporated, and the resultant residue was purified by column chromatography (hexane:ethyl acetate=7:3), to afford 120 mg of the title compound as a pale yellow oil.
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-4110f144624145549fb126ad24035122 |
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| Source note | uspto-grants-2008_09 |
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