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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606889Generated: October 27, 2026

Triethylamine → 2-Fluoro-5-(5-methoxypyridin-3-ylethynyl)-benzonitrile

https://huagongshe.com/reaction/606889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluoro-5-iodobenzonitrileHCID 2778928—
Reactant3-Ethynyl-5-methoxypyridineHCID 21097349—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178419050HCID 178419050—
Product2-Fluoro-5-(5-methoxypyridin-3-ylethynyl)-benzonitrileHCID 6704760990%

Reaction Conditions

Temperature60 °C

Reaction Steps

Add bis(triphenylphosphine)palladium (II) dichloride (77 mg, 0.1 mmol), copper (I) iodide (44 mg, 0.23 mmol), and 3-ethynyl-5-methoxypyridine (300 mg, 2.3 mmol), (prepared as described in PREPARATION 10), to a solution of 2-fluoro-5-iodobenzonitrile (670 mg, 2.7 mmol) in triethylamine (3.4 mL, 34 mmol) and heat at 60° C. for 2.75 h. Cool to room temperature and concentrate. Purify the residue by silica gel chromatography, eluting with 100:0 to 80:20 dichloromethane/ethyl acetate followed by a second silica gel chromatography, eluting with 75:25 to 60:40 hexanes:ethyl acetate to give the title compound as a white solid (510 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-7e0beb338e42442d8e7bf97e48221d7a
Source noteuspto-grants-2011_03