Reaction #1256772

ord-d30fbe2da0e64b85a81f62b3bb31ba9f

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    FiltrationAfter dilution with iPr2O the product was collected by filtration
  2. 2
    Washwashed with one portion of iPr2O
  3. 3
    Otherbefore drying it under high vacuum at 50° C.
  4. 4
    Otherto obtain 686 mg (79%) as a white solid

Procedure

{trans-4-[2-(4-Isoxazolo[4,5-c]pyridin-3-yl-piperazin-1-yl)-ethyl]-cyclohexyl}-carbamic acid tert-butyl ester (930 mg, 2.2 mmol) was dissolved in CH2Cl2 (3 ml) and 4 N HCl in dioxane (10.8 ml, 43 mmol) was added. The resulting mixture was stirred 16 h at r.t. After dilution with iPr2O the product was collected by filtration and washed with one portion of iPr2O before drying it under high vacuum at 50° C. to obtain 686 mg (79%) as a white solid. m/z=330.3 ([M+H]+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07825123B2uspto-grants-2010_11