Реакция #2254190

ord-3912cf40106a433cb14d95382a2ef007

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter 30 minutes at room temperature the reaction is quenched with water
  2. 2
    Экстракцияextracted three times with dichloromethane
  3. 3
    ПромывкаThe combined organic phases are washed with a saturated aqueous solution of NaCl
  4. 4
    Сушкаa saturated aqueous solution of NaHCO3, dried over Na2SO4
  5. 5
    Концентрированиеconcentrated in vacuo
  6. 6
    ДругоеThe crude product is purified on a semi-preparative reversed phase HPLC

Методика

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 Na2SO4 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09044389B2uspto-grants-2015_06