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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610129Generated: October 26, 2026

Water → 5-Bromo-3-(3-fluorophenyl)-7-methyl-1-trityl-1H-indazole

https://huagongshe.com/reaction/1610129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantTriphenylmethane chlorideHCID 22260971—
ReactantHCID 178422425HCID 178422425—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-3-(3-fluorophenyl)-7-methyl-1-trityl-1H-indazoleHCID 2226074042.4%

Reaction Steps

To a solution of 2.56 g of 5-bromo-3-(3-fluorophenyl)-7-methyl-1H-indazole in 30 ml of dimethylformamide was added 0.50 g of sodium hydride at room temperature, and the mixture was stirred at the same temperature for 15 minutes. At the same temperature, 2.34 g of triphenylmethane chloride was added and the mixture was stirred at the same temperature for one day. Water was added to the reaction mixture and the mixture was diluted with ethyl acetate. The organic layer was sequentially washed with saturated aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:10) and the resulting crystals were washed with diethyl ether, to give 1.94 g of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982274B2
Source datasetuspto-grants-2006_01
ORD IDord-6435ab83239c442aa72212c21448c09f
Source noteuspto-grants-2006_01