Reaktion #40514

ord-981b4dc1e0c84bf89a142b850617dd70

Reaktionsgleichung

O=C([O-])O.[Na+]
sodium bicarbonate
O=[N+]([O-])[O-].[Na+]
Sodium nitrate
Fc1cncc2[nH]c3ccc(Cl)cc3c12
Intermediate 65
Fc1cncc2[nH]c3ccc(Cl)cc3c12
6-Chloro-4-fluoro-9H-β-carboline
CO
methanol
O=[N+]([O-])c1cc(Cl)cc2c1[nH]c1cncc(F)c12
6-chloro-4-fluoro-8-nitro-9H-β-carboline
Ausbeute 102.2%

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas removed on a rotary evaporator
  2. 2
    Sonstigeto afford a crude solid which
  3. 3
    Filtrationthe precipitated solids were collected by suction filtration
  4. 4
    Waschenwashed with water (300 mL)
  5. 5
    Sonstigedried in vacuo

Vorschrift

Sodium nitrate (1.5 eq, 53 mmol, 4.5 g) was added portionwise to a solution of Intermediate 65 (1.0 eq, 35 mmol, 7.8 g) in trifluoroacetic acid (200 mL) and the resulting mixture heated at 70° C. for 3 h. After cooling to RT the trifluoroacetic acid was removed on a rotary evaporator to afford a crude solid which was suspended in a small volume of methanol and added dropwise to a vigorously stirred mixture of saturated sodium bicarbonate solution (500 mL). The resulting slurry was stirred for 15 min then the precipitated solids were collected by suction filtration, washed with water (300 mL) and then dried in vacuo to afford 6-chloro-4-fluoro-8-nitro-9H-β-carboline (about 9.5 g) which was used in the subsequent step without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07727985B2uspto-grants-2010_06