Reaction #1256770

ord-44572ec6024d4706b31180863e468c20

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 850 mg (97%) as a pink solid

Procedure

4-Isoxazolo[4,5-c]pyridin-3-yl-piperazine-1-carboxylic acid tert-butyl ester (960 mg, 3.1 mmol) was dissolved in CH2Cl2 (2 ml) and 4 N HCl in dioxane (15.7 ml, 63 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 850 mg (97%) as a pink solid. m/z=205.2 ([M+H]+).

Source

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