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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34038Generated: October 25, 2026

Triethylamine → 6-Fluoro-3-[(E)-2-(4-fluorophenyl)-vinyl]-5-nitro-1-trityl-1H-indazole

https://huagongshe.com/reaction/34038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-FluorostyreneHCID 67883—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant3-bromo-6-fluoro-5-nitro-1-trityl-1H-indazoleHCID 68928300—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product6-Fluoro-3-[(E)-2-(4-fluorophenyl)-vinyl]-5-nitro-1-trityl-1H-indazoleHCID 6892849246.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 600 mg of 3-bromo-6-fluoro-5-nitro-1-trityl-1H-indazole in 6 mL of N,N-dimethylformamide were successively added 292 mg of 4-fluorostyrene, 71 mg of 2-(di-tert-butylphosphino)biphenyl, 27 mg of palladium acetate (II) and 0.85 mL of triethylamine, and stirred at 80° C. for 6.5 hours. The solvent was evaporated, and the resulting residue was dissolved in 25 mL of ethyl acetate. The organic layer was successively washed with water (twice) and saturated brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated. The obtained crude crystal was recrystallized from ethyl acetate-diisopropylether, to afford 304 mg of the title compound as bright yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-3c4fee8c4bba47369bf067c0e1d01924
Source noteuspto-grants-2008_09