Реакция #6978

ord-462377d8589748f69115599778a6a316

Уравнение реакции

O=[N+]([O-])O
nitric acid
O=S(=O)(O)O
H2SO4
O=S(=O)(Cl)c1ccc(F)cc1
4-fluorobenzenesulfonyl chloride
CCN(C(C)C)C(C)C
DIPEA
O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
NC1CC1
cyclopropylamine
O=[N+]([O-])c1cc(S(=O)(=O)NC2CC2)ccc1F
N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide
Выход 92.0%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONpoured
  2. 2
    Экстракцияextracted with dichloromethane (2×)
  3. 3
    ПромывкаThe organic layer was washed with brine
  4. 4
    Сушкаdried over Na2SO4
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated
  7. 7
    workup.DISSOLUTIONThe residue was dissolved in CH2Cl2 (30 mL)
  8. 8
    Температураcooled to −40° C.
  9. 9
    workup.ADDITIONwere added
  10. 10
    workup.STIRRINGAfter stirring at −40° C. for 2 h
  11. 11
    Экстракцияextracted with dichloromethane
  12. 12
    ДругоеThe organic layer was separated
  13. 13
    Концентрированиеconcentrated in vacuo

Методика

To a solution of fuming nitric acid (8 mL) and conc. H2SO4 (16 mL), was added 4-fluorobenzenesulfonyl chloride (1.3 g, 6.7 mmol) in small portions. The mixture was stirred at RT for 2 h. and then poured onto crushed ice (60 g) and extracted with dichloromethane (2×). The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was dissolved in CH2Cl2 (30 mL) cooled to −40° C. and cyclopropylamine (388 mg, 6.8 mmol), followed by DIPEA (8 mmol) were added. After stirring at −40° C. for 2 h, the mixture was poured on 5% citric acid solution and extracted with dichloromethane. The organic layer was separated, and passed through a short pad of silica gel and concentrated in vacuo to afford N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide (1.6 g, 92%) as a yellow solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07084160B2uspto-grants-2006_08