Reaktion #1129455

ord-6516a53259c5435e9f881a76fbbe0139

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto give a dark suspension
  2. 2
    SonstigeThe suspension was sonicated for 2 min
  3. 3
    SonstigeThe reaction mixture was sonicated again for 2 min
  4. 4
    workup.STIRRINGstirred at RT for 10 min
  5. 5
    Extraktionextracted with 3:1 CHCl3
  6. 6
    WaschenThe combined organic layers were washed with satd NaCl
  7. 7
    Trocknendried over Na2SO4
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated in vacuo
  10. 10
    Sonstigeto give 840 mg crude product
  11. 11
    Sonstigechromatographed through a Redi-Sep® pre-packed silica gel column (80 g)
  12. 12
    Wascheneluting with a gradient of 10% to 50% EtOAc in CH2Cl2

Vorschrift

A mixture of 4-(5-amino-6-methylisoquinolin-1-ylamino)benzonitrile (0.250 g, 0.91 mmol) and 9-(4-methoxybenzyl)-6-(2-fluoropyridin-3-yl)-9H-purine (0.34 g, 1.0 mmol) in anhydrous THF (20 mL) was treated dropwise with lithium bis(trimethylsilyl)amide (1.0 M solution in THF; 2.7 mlL, 2.7 mmol) to give a dark suspension. The suspension was sonicated for 2 min and then stirred at RT for 30 min. The reaction mixture was sonicated again for 2 min. The mixture was treated with 1N aq HCl (5 mL) and stirred at RT for 10 min. The reaction mixture was added to satd NaHCO3 (70 mL) and extracted with 3:1 CHCl3:IPA (3×50 mL). The combined organic layers were washed with satd NaCl, dried over Na2SO4, filtered, and concentrated in vacuo to give 840 mg crude product. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep® pre-packed silica gel column (80 g), eluting with a gradient of 10% to 50% EtOAc in CH2Cl2, to give 4-(5-(3-(9-(4-methoxybenzyl)-9H-purin-6-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile. MS (ESI, pos. ion) m/z: 590.2 [M+H]+

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08557830B2uspto-grants-2013_10