Réaction #69271

ord-c25229f019e0435fbf60b70be383dcf5

Solvants

Conditions de réaction

Température
-78°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreprepared
  2. 2
    Températureto warm to 0° C.
  3. 3
    workup.STIRRINGThe reaction was stirred at room temperature overnight
  4. 4
    Autrepartitioned between ethyl acetate and water
  5. 5
    LavageThe organic layer was washed with saturated NaCl
  6. 6
    Séchagedried over MgSO4
  7. 7
    Filtrationfiltered
  8. 8
    Concentrationconcentrated
  9. 9
    Autreto give the crude product
  10. 10
    AutreThe crude product was purified

Mode opératoire

1 M Diisobutylaluminum hydride in hexane (0.31 mL) was added dropwise to a solution of methyl 3-(3-cyanophenyl)-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanoate (100 mg, 0.0002 mol) (prepared by using a procedure analogous to Example 712, Step 1) in DCM (3 mL, 0.05 mol) and the mixture was cooled to −78° C. The reaction mixture was stirred at −78° C. for 4 h and was afterward quenched with cold methanol (3 mL, 0.07 mol). The reaction was allowed to warm to 0° C. and potassium carbonate (60 mg, 0.0004 mol) and Bestmann-Ohira reagent (1.5 eq, 57 mg) (E. Quesada et al, Tetrahedron, 62 (2006) 6673-6680) were added. The reaction was stirred at room temperature overnight, and then partitioned between ethyl acetate and water. The organic layer was washed with saturated NaCl, dried over MgSO4, filtered and concentrated to give the crude product. The crude product was purified using silica gel (EtOAC/Hexane 1:3 to 1:1) to give the desired product, 3-{1-[4-(7-{[2-(trimethylsilyl)ethoxy]-methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]but-3-yn-1-yl}benzonitrile (40 mg of mixture). m/z=469 (M+1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08530485B2uspto-grants-2013_09