Reaktion #470985

ord-200b01f2651f4333a3c643cef6cf4155

Reaktionsgleichung

O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1
2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl
CCOC(=O)c1cc2cccc(Br)c2o1
Ethyl 7-bromobenzofuran-2-carboxylate
c1ccc(CCN2CCNCC2)nc1
1-(2-(pyridin-2-yl)ethyl)piperazine
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
title compound
Ausbeute 40.0%
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Ethyl 7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate
Ausbeute 40.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
95°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigein dry
  2. 2
    Sonstigedegassed dioxane (13 mL)
  3. 3
    Sonstigethe layers were separated
  4. 4
    ExtraktionThe aq phase was extracted with DCM (3×)
  5. 5
    WaschenThe combined organic phases were washed with water
  6. 6
    Trocknendried (MgSO4)
  7. 7
    Filtrationfiltered
  8. 8
    Sonstigeevaporated
  9. 9
    SonstigeThe crude product was purified by flash chromatography

Vorschrift

Ethyl 7-bromobenzofuran-2-carboxylate (0.900 g, 3.34 mmol) and 1-(2-(pyridin-2-yl)ethyl)piperazine (0.672 g, 3.51 mmol) were mixed in dry degassed dioxane (13 mL). To this mixture cesium carbonate (1.417 g, 4.35 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (0.159 g, 0.33 mmol) and tris(dibenzylideneacetone)dipalladium(0) (0.153 g, 0.17 mmol) were added under argon and the reaction was heated at 95° C. over night. Water and DCM were added and the layers were separated. The aq phase was extracted with DCM (3×). The combined organic phases were washed with water, dried (MgSO4), filtered and evaporated. The crude product was purified by flash chromatography. (SiO2; DCM/MeOH 95/5) to give 0.507 g (40%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08367676B2uspto-grants-2013_02