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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
ReactantPhosphine, tris(4-methylphenyl)-HCID 13956—
Reactant3-vinyl-4-methoxy-1-trityl-1H-indazole-5-carbonitrileHCID 23070127—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
Product4-Methoxy-3-[(E)-2-(pyridin-3-yl)-vinyl]-1-trityl-1H-indazole-5-carbonitrileHCID 68928542—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-4110f144624145549fb126ad24035122
Source noteuspto-grants-2008_09