Reaktion #9761

ord-29ab68ec7fbd4c80a56aeb3f91a16063

Reaktionsgleichung

CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc(C)c(CCc2ccc(OCC34OCC(C)(CO3)CO4)c(C)c2)s1
tributyl[4-methyl-5-(2-{3-methyl-4-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methoxy]phenyl}ethyl)thien-2-yl]stannane
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc(C)c(CCc2ccc(OCC34OCC(C)(CO3)CO4)c(C)c2)s1
intermediate 100
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cc(C)c(CCc2ccc(OCC34OCC(C)(CO3)CO4)c(C)c2)s1
tributyl[4-methyl-5-(2-{3-methyl-4-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methoxy]phenyl}ethyl)thien-2-yl]stannane
N#Cc1ccc(Br)cc1F
2-fluoro-4-bromobenzonitrile
c1coc(P(c2ccco2)c2ccco2)c1
trifuranyl phosphine
Cc1cc(CCc2sc(-c3ccc(C#N)c(F)c3)cc2C)ccc1OCC12OCC(C)(CO1)CO2
title compound
Cc1cc(CCc2sc(-c3ccc(C#N)c(F)c3)cc2C)ccc1OCC12OCC(C)(CO1)CO2
2-fluoro-4-[4-methyl-5-(2-{3-methyl-4-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methoxy]phenyl}ethyl)thien-2-yl]benzonitrile

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 3 hours
  2. 2
    SonstigeThe solvent was removed
  3. 3
    Sonstigethe residue purified by Biotage® chromatography
  4. 4
    workup.ADDITIONa mixture of petroleum ether:ethyl acetate (4:1) as eluent

Vorschrift

A mixture of tributyl[4-methyl-5-(2-{3-methyl-4-[(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)methoxy]phenyl}ethyl)thien-2-yl]stannane (intermediate 100, 0.037 g) and 2-fluoro-4-bromobenzonitrile (0.011 g) in tetrahydrofuran (2 ml) was treated with palladium bis(dibenzylideneacetone) (0.0035 g) and trifuranyl phosphine (0.0013 g) and the resulting mixture stirred at reflux for 3 hours. The solvent was removed and the residue purified by Biotage® chromatography using a mixture of petroleum ether:ethyl acetate (4:1) as eluent to give the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091237B2uspto-grants-2006_08