Реакция #158435

ord-957c87e2f559490088975bb6ae725bfd

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe mixture was stirred at room temp for 18 hrs
  2. 2
    ДругоеIt was partitioned between EtOAc and water
  3. 3
    Экстракцияthe aqueous layer was extracted with EtOAc once more
  4. 4
    ПромывкаCombined extracts were washed with Na2SO4
  5. 5
    Другоеevaporated
  6. 6
    Другоеto give an oily residue
  7. 7
    ДругоеIt was purified by Combiflash (24 g silica gel)
  8. 8
    Промывкаeluting with 3:7

Методика

To a solution of 4-(6-phenyl-1,4-dioxaspiro[4.5]decan-6-yl)butanoic acid (62.0 mg, 0.204 mmol) and (R,Z)-4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-N′-hydroxy-3,5-dimethylbenzimidamide (50 mg, 0.17 mmol) in acetonitrile (2 mL) was added N,N′-diisopropylcarbodiimide (0.032 mL, 0.204 mmol), and the mixture was stirred for 1 hr at room temp. Then 1M TBAF (0.221 mL, 0.221 mmol) was added, and the mixture was stirred at room temp for 18 hrs. It was partitioned between EtOAc and water, and the aqueous layer was extracted with EtOAc once more. Combined extracts were washed with Na2SO4 and evaporated to give an oily residue. It was purified by Combiflash (24 g silica gel) eluting with 3:7 followed by 1:1 EtOAc-hexane to give 3-(4-(((R)-2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-3,5-dimethylphenyl)-5-(3-(6-phenyl-1,4-dioxaspiro[4.5]decan-6-yl)propyl)-1,2,4-oxadiazole as an oil (57 mg). LC/MS: m/e 563.21 (M+H)+.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822510B2uspto-grants-2014_09