Réaction #10193

ord-a0e1cb1ebb244b41a71131589d967acf

Équation de réaction

Cl
HCl
Cl
HCl
Nc1ccc2c(c1)C1CC2CN(C(=O)C(F)(F)F)C1
1-(4-Amino-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone
O=N[O-].[Na+]
sodium nitrite
O=C(N1CC2CC(C1)c1cc(Cl)ccc12)C(F)(F)F
oil
Rendement 95.0%
O=C(N1CC2CC(C1)c1cc(Cl)ccc12)C(F)(F)F
1-(4-Chloro-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone
Rendement 95.0%

Solvants

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas cooled to room temperature
  2. 2
    Extractionextracted with ethyl acetate (4×30 mL)
  3. 3
    SéchageAfter drying over Na2SO4
  4. 4
    Filtrationthe solution was filtered
  5. 5
    Concentrationconcentrated to an oil which
  6. 6
    Filtrationwas filtered through a Silica pad
  7. 7
    Autreto remove baseline material
  8. 8
    Lavageeluting with 50% ethyl acetate/hexanes

Mode opératoire

1-(4-Amino-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone (460 mg, 1.7 mmol) was dissolved in H2O (2 mL) and concentrated HCl solution(1 mL) then cooled to 0° C. and treated with a solution of sodium nitrite (NaNO2) (275 mg) in H2O (1 mL) dropwise. To the resulting solution was added a CuCl (202 mg, prepared as described above, 2.04 mmol) in concentrated HCl solution (2 mL) over 10 minutes (gas evolution observed). The resulting solution was warmed to 60° C. for 15 minutes, then was cooled to room temperature and extracted with ethyl acetate (4×30 mL). After drying over Na2SO4, the solution was filtered and concentrated to an oil which was filtered through a Silica pad to remove baseline material eluting with 50% ethyl acetate/hexanes to give an oil (470 mg, 95%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07091372B2uspto-grants-2006_08