반응 #73843

ord-a6954906923247e688a5b7085299de23

반응 방정식

Clc1nccnc1Cl
2,3-dichloropyrazine
OB(O)c1ccc(F)cc1
4-fluorophenyl boronic acid
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
C1CCC(P(C2CCCCC2)C2CCCCC2)CC1
tricyclohexylphosphine
Fc1ccc(-c2nccnc2Cl)cc1
2-chloro-3-(4-fluorophenyl)pyrazine
수율 55.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwere added
  2. 2
    기타they were reacted at 85° C. for 11 hours
  3. 3
    기타After the reaction
  4. 4
    여과filtrated
  5. 5
    workup.DISTILLATIONA solvent of the obtained filtrate was distilled off

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541574B2uspto-grants-2013_09