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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891492Generated: November 1, 2026

Nitrogen → 2-Fluoro-5-(thiazol-5-yl)benzonitrile

https://huagongshe.com/reaction/1891492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant5-(Tributylstannyl)-1,3-thiazoleHCID 2763257—
Reactant2-Fluoro-5-iodobenzonitrileHCID 2778928—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-(thiazol-5-yl)benzonitrileHCID 6719161482%

Reaction Conditions

Temperature85 °C

Reaction Steps

To 5-(tributylstannyl)thiazole (1.00 g, 2.7 mmol) in THF (10 mL) was added 2-fluoro-5-iodobenzonitrile (0.791 g, 3.2 mmol). The solution was degassed with N2 and bis(triphenylphosphine)palladium(II) chloride Pd(Ph)2Cl2 (0.187 g, 0.27 mmol) was added. The solution was further degassed for five minutes before heating to 85° C. for 2 h. Upon cooling, the reaction mixture was diluted with saturated NaHCO3 and washed with EA (3×50 mL). The combined organic layers were dried over MgSO4, filtered, and concentrated. The crude product was purified by chromatography (10% EA/Hexanes) to afford 0.450 g (82%) of 2-fluoro-5-(thiazol-5-yl)benzonitrile THZ INT-3 as a tan solid. LCMS-ESI (m/z) calculated for C10H5FN2S: 204.2; found 205.0 [M+H]+, tR=3.00 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507538B2
Source datasetuspto-grants-2013_08
ORD IDord-532c777ab778463fbccc212e606e4a00
Source noteuspto-grants-2013_08