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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45565Generated: October 25, 2026

Cesium carbonate → 2-Chloro-3-(4-fluorophenyl)pyrazine

https://huagongshe.com/reaction/45565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTricyclohexylphosphineHCID 75806—
Reactant2,3-DichloropyrazineHCID 78575—
Reactant4-Fluorophenylboronic acidHCID 285645—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-3-(4-fluorophenyl)pyrazineHCID 5986625855%

Reaction Steps

First, 5.06 g of 2,3-dichloropyrazine, 5.23 g of 4-fluorophenyl boronic acid, 22.16 g of cesium carbonate, and 200 mL of dioxane were put in a three-neck flask equipped with a reflux pipe, and 0.467 g of tris(dibenzylideneacetone)dipalladium(0) (abbreviation: Pd2(dba)3) and 2.5 mL of tricyclohexylphosphine (abbreviation: Cy3P) were added thereto while the mixture was stirred under a nitrogen atmosphere, and they were reacted at 85° C. for 11 hours. After the reaction, the reaction solution was cooled down to room temperature and filtrated. A solvent of the obtained filtrate was distilled off, and the obtained residue was refined with a column chromatography using dichloromethane as a development solvent, so that 2-chloro-3-(4-fluorophenyl)pyrazine was obtained (light yellow powder, yield: 55%). A synthesis scheme of Step 1 is shown by the following (a1-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541574B2
Source datasetuspto-grants-2013_09
ORD IDord-a6954906923247e688a5b7085299de23
Source noteuspto-grants-2013_09