Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334792Generated: October 28, 2026

3-Fluoro-2-iodopyridine → 2-(4-(3-Fluoropyridin-2-yl)but-3-ynyl)benzo[d]oxazole

https://huagongshe.com/reaction/334792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-2-iodopyridineHCID 1519483—
Reactant2-(But-3-ynyl)benzo[d]oxazoleHCID 86086907—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-(4-(3-Fluoropyridin-2-yl)but-3-ynyl)benzo[d]oxazoleHCID 6667558415.2%

Reaction Steps

In a dry reaction tube containing in suspension copper iodide (28 mg, 0.148 mol) and triethylamine (8.30 mL, 59.20 mmol), were added 3-fluoro-2-iodopyridine (660 mg, 2.96 mmol) and Pd(PPh3)2Cl2 (104 mg, 0.148 mmol) under N2. A yellow suspension was obtained. After a 5 minutes of stirring at room temperature, was added a solution 2-(But-3-ynyl)benzo[d]oxazole (compound 8(A), 510 mg, 3 mmol) in triethylamine (0.2 mL) under N2. Immediately the color of the reaction turns to black. The mixture was stirred at room temperature for 30 min and heated at 50° C. overnight under N2. Triethylamine was removed under reduce pressure and the crude product was purified by flash chromatography (Prepacked column 50 g, Cyclohexane/AcOEt: 60/40 as eluent) following by C18 chromatography (Prepacked column 15 g, H2O/CH3CN: from 80/20 to 40/600 as eluent) to afford 120 mg of 2-(4-(3-fluoropyridin-2-yl)but-3-ynyl)benzo[d]oxazole (Yield: 15%) as white powder (Mp=86-88° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-e14e994e76084d638e7cd590dc5ffb89
Source noteuspto-grants-2014_11