Реакция #77834

ord-548d4312cc224e57adc1d3f3ab1ca060

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаthe solution was washed with 1N HCl
  2. 2
    СушкаThe EtOAc was dried
  3. 3
    Фильтрацияfiltered
  4. 4
    Концентрированиеconcentrated
  5. 5
    ДругоеReverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue

Методика

N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide, (61b), (100 mg) was dissolved in DMF (3 mL) prior to the addition of 4-methylmorpholine (0.13 mL) and 2-trifluoromethylphenyl isocyanate (0.05 mL). After stirring overnight, EtOAc was added and the solution was washed with 1N HCl. The EtOAc was dried, filtered, and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title benzamide (50 mg). MS found: (M+Na)+=564.3.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06706712B2uspto-grants-2004_03