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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677675Generated: October 31, 2026

4-Fluoroiodobenzene → 1-(4-Fluorophenyl)-1H-indazole-4-carboxylic acid 3-trifluoromethyl-benzylamide

https://huagongshe.com/reaction/1677675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroiodobenzeneHCID 9605—
ReactantPotassium CarbonateHCID 11430—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant1H-indazole-4-carboxylic acid 3-trifluoromethyl-benzylamideHCID 58138854—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(4-Fluorophenyl)-1H-indazole-4-carboxylic acid 3-trifluoromethyl-benzylamideHCID 58138826—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1H-indazole-4-carboxylic acid 3-trifluoromethyl-benzylamide (1.1 g, 3.4 mmol), copper(I) iodide (0.005 g, 0.02 mmol), potassium carbonate (0.04 g, 0.3 mmol) and 4-fluoroiodobenzene (0.04 g, 0.2 mmol) were charged in a sealed tube at room temperature. The tube was evacuated and back-filled with argon. The solids were dissolved in DMF (6 mL) and the resultant solution was treated with rac-trans-N,N′-dimethylcyclohexane-1,2-diamine (0.005 g, 0.04 mmol). The solution was stirred at 120° C. for 3 hours and cooled to room temperature. The solution was diluted with water (15 mL) and ethyl acetate (30 mL). The organic layer was separated, washed with brine and dried over sodium sulfate. The solvent was removed in vacuo. The crude residue was purified by silica gel chromatography eluting with a gradient of 10-40% ethyl acetate in hexanes to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008327B2
Source datasetuspto-grants-2011_08
ORD IDord-d4a8bbd1a91048499ab5f244d91eb89f
Source noteuspto-grants-2011_08