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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098831Generated: October 26, 2026

Pyridine → 1-(4-Fluorophenyl)-5-iodo-6-methylindazole

https://huagongshe.com/reaction/1098831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant5-iodo-6-methyl-1H-indazoleHCID 59339696—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product1-(4-Fluorophenyl)-5-iodo-6-methylindazoleHCID 5933991451.1%

Reaction Steps

5-Iodo-6-methylindazole (1.3 g, 5.0 mmol), p-fluorobenzeneboronic acid (1.4 g, 10 mmol), anhydrous copper(II) acetate (1.4 g, 7.5 mmol) and pyridine (0.80 mL, 10 mmol) were stirred in dichloromethane (30 mL) overnight. Additional portions of p-fluorobenzeneboronic acid (0.47 g, 3.4 mmol), anhydrous copper(II) acetate (0.45 g, 2.5 mmol) and pyridine (0.27 mL, 3.4 mmol) were added. The mixture was filtered through celite after stirring for an additional night. The filtrate was concentrated and purified by column chromatography (SiO2, toluene) to give the subtitle compound (0.90 g, 51%) as a light orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143290B2
Source datasetuspto-grants-2012_03
ORD IDord-2ddaf770e336452fa64a04bd6a684a14
Source noteuspto-grants-2012_03