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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606864Generated: October 26, 2026

Diethylamine → 5-(3-Hydroxy-4-fluorophenylethynyl)-nicotinonitrile

https://huagongshe.com/reaction/606864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant5-EthynylnicotinonitrileHCID 22416563—
Reactant2-Fluoro-5-iodophenolHCID 46911832—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product5-(3-Hydroxy-4-fluorophenylethynyl)-nicotinonitrileHCID 6704781442%

Reaction Conditions

Temperature60 °C

Reaction Steps

Add bis(phenylnitrile)palladium (II) chloride (115 mg, 0.3 mmol) to a suspension of copper (I) iodide (38 mg, 0.2 mmol) in anhydrous 1,4-dioxane (1 mL) under nitrogen and stir for 10 min. Sequentially add 5-ethynyl-nicotinonitrile (1.28 g, 10 mmol), (prepared essentially as described in PREPARATION 4), 2-fluoro-5-iodophenol, (prepared essentially as described in PREPARATION 15), (2.37 g, 10 mmol) and tri-tert-butylphosphine (121 mg, 0.6 mmol) in 1,4-dioxane (5 mL) and diethylamine (2.1 mL, 12 mmol) to the reaction mixture and heat at 60° C. for 16 h. Cool to room temperature, dilute with diethyl ether, stir for 10 min and filter through diatomaceous earth. Wash the filtrate sequentially with water and an aqueous saturated solution of sodium chloride. Dry (magnesium sulfate), concentrate and purify by silica gel chromatography, eluting with 0:100 to 35:100 ethyl acetate:hexanes, to give the title compound (1.0 g, 42%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-c26e31154fe543f8a304049fba5b5ba6
Source noteuspto-grants-2011_03