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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423075Generated: November 1, 2026

Pyridine → 4-Bromo-5-fluoro-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazole

https://huagongshe.com/reaction/2423075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBoronic AcidHCID 61668—
Reactant4-Benzyloxy-3-fluorophenylboronic AcidHCID 2737788—
Reactant4-Bromo-5-fluoro-1H-indazoleHCID 59272979—
CatalystCupric acetateHCID 8895—
Product4-Bromo-5-fluoro-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazoleHCID 5927295949.7%

Reaction Steps

A mixture of 4-bromo-5-fluoro-1H-indazole (D15) (1.008 g, 4.69 mmol), {3-fluoro-4-[(phenylmethyl)oxy]phenyl}boronic acid 1.730 g, 7.03 mmol), copper(II) acetate (1.277 g, 7.03 mmol) and pyridine (0.758 mL, 0.742 g, 9.38 mmol) were stirred together vigorously under an air atmosphere with powdered 4A molecular sieves (5 g) at room temperature. After 6 days another 580 mg of boronic acid were added and stirring continued for a further 24 hrs. The mixture was filtered through celite, the celite was washed with dichloromethane and the combined filtrate was washed with water, dried over Na2SO4 and evaporated. Chromatography (silica gel, 0-100% dichloromethane in isohexane), followed by trituration of the product with diethyl ether gave the title compound (D16) (0.968 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960563B2
Source datasetuspto-grants-2011_06
ORD IDord-5178476d3d7c460bb5fc025e7ee1b0d6
Source noteuspto-grants-2011_06