Réaction #477957

ord-f508d143cc1a47d48746877f0229176e

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter 30 minutes at room temperature the reaction is quenched with water
  2. 2
    Extractionextracted three times with dichloromethane
  3. 3
    LavageThe combined organic phases are washed with a saturated aqueous solution of NaCl
  4. 4
    Séchagea saturated aqueous solution of NaHCO3, dried over NazSO4
  5. 5
    Concentrationconcentrated in vacuo
  6. 6
    AutreThe crude product is purified on a semi-preparative reversed phase HPLC

Mode opératoire

DIPEA (0.246 ml) is added to a solution of (2,2,2-trifluoro-ethylcarbamoyl)-methyl-ammonium trifluoroacetate (0.170 g, Example 4, step B), PYBOP (0.270 g), and 5-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-3-methyl-thiophene-2-carboxylic acid (0.2 g) in dichloromethane (3 ml) at 0° C. After 30 minutes at room temperature the reaction is quenched with water and extracted three times with dichloromethane. The combined organic phases are washed with a saturated aqueous solution of NaCl and a saturated aqueous solution of NaHCO3, dried over NazSO4 and concentrated in vacuo. The crude product is purified on a semi-preparative reversed phase HPLC to yield 5-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]3-methyl-thiophene-2-carboxylic acid [(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-amide (8.73 g) as a beige foam. MS (HPLC/MS): 562 (MH+), Retention time: 3.94 min.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08383659B2uspto-grants-2013_02