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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13066Generated: October 25, 2026

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

https://huagongshe.com/reaction/13066

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 numberUS07728030B2
Source datasetuspto-grants-2010_06
ORD IDord-72bb574897744091b253023ce7c3b848
Source noteuspto-grants-2010_06