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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811921Generated: October 30, 2026

2-Fluoro-3-(tributylstannyl)pyrazine → 4-(3-Fluoropyrazin-2-yl)-2-methyl-6-(methylthio)pyrimidine

https://huagongshe.com/reaction/1811921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-3-(tributylstannyl)pyrazineHCID 12130662—
Reactant4-Iodo-2-methyl-6-(methylthio)pyrimidineHCID 77231267—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-(3-Fluoropyrazin-2-yl)-2-methyl-6-(methylthio)pyrimidineHCID 6660022012%

Reaction Conditions

Temperature140 °C

Reaction Steps

A glass microwave reaction vessel was charged with 4-iodo-2-methyl-6-(methylthio)pyrimidine (266 mg, 1.000 mmol), 2-fluoro-3-(tributylstannyl)pyrazine (387 mg, 1.000 mmol) and tetrakis(triphenylphosphine)palladium(0) (116 mg, 0.100 mmol) in toluene (3 mL). The reaction mixture was stirred and heated in an Emrys Optimizer microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 140° C. for 40 min. The solvent was removed in vacuo and the residue was purified by silica gel chromatography eluting with 40% EtOAc/hexanes to give 4-(3-fluoropyrazin-2-yl)-2-methyl-6-(methylthio)pyrimidine (28 mg, 0.119 mmol, 12% yield). 1H NMR (300 MHz, CDCl3) δ 8.68 (s, 1H); 8.32 (s, 1H); 7.67 (s, 1H); 2.79 (s, 3H); 2.63 (s, 3H). m/z (ESI, +ve ion) 237.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-e08cd59deb714e8189ecff4fd74e740e
Source noteuspto-grants-2013_01