Reaktion #959702

Reaktionsgleichung

2-(1-hydroxy-2-methylpropan-2-yl)isoindoline-1,3-dione

2-methyl-4-(1H-pyrazol-3-yl)benzonitrile

triphenylphosphine

DIAD

Triphenylphosphine

DIAD

→

title product

Ausbeute 16.3%

4-(1-(2-(1,3-dioxoisoindolin-2-yl)-2-methylpropyl)-1H-pyrazol-3-yl)-2-methylbenzonitrile

Ausbeute 16.3%

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred at RT for 2 days
2. 2
   Temperaturrefluxed for 2 hours
3. 3
   SonstigeSolvent was evaporated
4. 4
   workup.ADDITION50 ml of water was added
5. 5
   Waschenthe mixture was washed with 3×50 ml of DCM
6. 6
   Trocknendried over Na2SO4
7. 7
   Filtrationfiltered
8. 8
   Sonstigeevaporated to dryness
9. 9
   SonstigeThe crude mixture was purified twice by CombiFlash (column: silica, eluent 0-100% EtOAc in heptane)

Vorschrift

2-(1-hydroxy-2-methylpropan-2-yl)isoindoline-1,3-dione (1.10 g; 5 mmol) and 2-methyl-4-(1H-pyrazol-3-yl)benzonitrile (0.366 g; 2.0 mmol) were dissolved in 5 ml of THF under nitrogen atmosphere. Triphenylphosphine (1.05 g; 4.0 mmol) and DIAD (0.79 ml; 4.0 mmol) were added and the reaction stirred at RT over the weekend. Additional triphenylphosphine (0.525 g; 2.0 mmol) and DIAD (0.39 ml; 2.0 mmol) were added and the mixture was stirred at RT for 2 days and then refluxed for 2 hours. Solvent was evaporated, 50 ml of water was added and the mixture was washed with 3×50 ml of DCM, dried over Na2SO4, filtered and evaporated to dryness. The crude mixture was purified twice by CombiFlash (column: silica, eluent 0-100% EtOAc in heptane) to obtain 125 mg (16%) of the title product. 1H-NMR (400 MHz; CDCl3): δ 1.56 (s, 6H), 2.60 (s, 3H), 4.2-4.38 (m, 2H), 6.50 (d, 1H), 7.33-7.87 (m, 8H).

Quelle