Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606939Generated: October 27, 2026

Triethylamine → 2-Fluoro-5-(5-methoxypyridin-3-ylethynyl)-benzoic acid

https://huagongshe.com/reaction/606939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluoro-5-iodobenzoic acidHCID 2778925—
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)-benzoic acidHCID 6704775954.4%

Reaction Steps

Add bis(triphenylphosphine)palladium (II) dichloride (70 mg, 0.10 mmol), copper (I) iodide (38 mg, 0.20 mmol), and 3-ethynyl-5-methoxypyridine, (prepared as described in PREPARATION 10), (400 mg, 3.0 mmol) to a solution of 2-fluoro-5-iodobenzoic acid (0.53 g, 2.0 mmol) in triethylamine (4.2 mL, 30.0 mmol) and stir at room temperature for 1 h. Heat at 50° C. for 18 h. Cool to room temperature and concentrate. Purify by silica gel chromatography, eluting with 100:0 to 60:40 ethyl acetate:methanol. Triturate the resulting solid with 3:1 hexanes:methanol to give the title compound as an off-white solid (295 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-cf46995eddec4883b9ee02bc24a1c525
Source noteuspto-grants-2011_03