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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983457Generated: October 30, 2026

Tributylphenyltin → 3-Phenyl-1H-5-indazolecarbonitrile

https://huagongshe.com/reaction/1983457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphenyltinHCID 607632—
Reactanttert-Butyl 3-bromo-5-cyano-1H-indazole-1-carboxylateHCID 22260825—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-Phenyl-1H-5-indazolecarbonitrileHCID 1306695657.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 300 mg of tert-butyl 3-bromo-5-cyano-1H-1-indazolecarboxylate produced in Production Example I-14-b in 10 ml dimethylformamide were added 376 mg of tri-n-butyl (phenyl)tin and 54 mg of tetrakis(triphenylphosphine)palladium(0), and the mixture was stirred at 150° C. for 45 minutes. After removing the solvent by distillation, the residue was dissolved in 1.5 ml of ethyl acetate and the mixture was adsorbed by 1.5 g of silica gel. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:toluene=3:97 to 1:19) and the resulting amorphous powder was crystallized from diisopropyl ether, to give 117 mg of the title compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541376B2
Source datasetuspto-grants-2009_06
ORD IDord-0943c8067863405fa208ca4de3a4a587
Source noteuspto-grants-2009_06