Réaction #8345

ord-2037d4dea16e4b4ca6ee4112e129ee14

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture is cooled
  2. 2
    Concentrationconcentrated in vacuo
  3. 3
    AutreThe residue is chromatographed on SiO2 (100% ethyl acetate to 10% methanol in ethyl acetate)

Mode opératoire

A solution of 7-(3-chloro-propoxy)-4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline (54 mg, 0.13 mmol), sodium iodide (5 mg, 0.03 mmol), and 2 N dimethylamine in tetrahydrofuran (3 mL, 6 mmol) in N,N-dimethylformamide (5 mL) is heated at 100° C. for 48 h. The mixture is cooled and concentrated in vacuo. The residue is chromatographed on SiO2 (100% ethyl acetate to 10% methanol in ethyl acetate) to yield the title compound, 41 mg (74%), as a brown solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07087626B2uspto-grants-2006_08