Реакция #41882

ord-e262cc0b3bfd400aae43afd37cfb4ac7

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ПромывкаThe organic layer was washed with brine
  2. 2
    Другоеdried
  3. 3
    Другоеevaporated
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in 15 mL DMF
  5. 5
    workup.ADDITIONpotassium carbonate (4.1 g) added
  6. 6
    workup.STIRRINGThe mixture stirred at rt for 3 h
  7. 7
    workup.ADDITIONwas poured onto water and EtOAc
  8. 8
    ПромывкаThe organic was washed with 1N HCl
  9. 9
    Другоеdried
  10. 10
    Другоеevaporated
  11. 11
    ДругоеThe residue was purified over silica (hexanes-EtOAc-2M ammonia in MeOH)

Методика

(S)-6-amino-7-hydroxy-3,4-dihydro-1H-isoquinoline-2,3-dicarboxylic acid 2-isopropyl ester 3-methyl ester (1.8 g) was dissolved in 10 mL EtOAc, 20 mL water and 5.0 g sodium bicarbonate added. 2-Chloro-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-acetyl chloride in 10 mL of EtOAc was added and the mixture stirred at rt for 1.5 h. The organic layer was washed with brine, dried and evaporated. The residue was dissolved in 15 mL DMF and potassium carbonate (4.1 g) added. The mixture stirred at rt for 3 h and was poured onto water and EtOAc. The organic was washed with 1N HCl, dried and evaporated. The residue was purified over silica (hexanes-EtOAc-2M ammonia in MeOH) to provide (S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-2-oxo-1,2,3,5,7,8-hexahydro-4-oxa-1,6-diaza-anthracene-6,7-dicarboxylic acid 6-isopropyl ester 7-methyl ester (2.0 g). LC-MS (m/z) 600.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07727983B2uspto-grants-2010_06