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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34100Generated: October 30, 2026

Triethylamine → HCID 68930524, compound

https://huagongshe.com/reaction/34100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Benzodioxole, 5-ethenyl-HCID 138986—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 68930344HCID 68930344—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
ProductHCID 68930524HCID 6893052413.8%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-af27b6d4d3c5467d8b3bbf7ae2b1d0c2
Source noteuspto-grants-2008_09