Reacción #595411

ord-bbebfcfa563e4092aa39103dae4d5b1c

Ecuación de reacción

Brc1ccc2[nH]c3ccc(Br)cc3c2c1
3,6-Dibromocarbazole
[N-]=[N+]=[N-].[Na+]
NaN3
O=C(O)[C@@H]1CCCN1
L-proline
[Na+].[OH-]
NaOH
[N-]=[N+]=Nc1ccc2[nH]c3ccc(Br)cc3c2c1
desired product
[N-]=[N+]=Nc1ccc2[nH]c3ccc(Br)cc3c2c1
3-azido-6-bromo-9H-carbazole

Disolventes

Condiciones de reacción

Temperatura
95°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe completed reaction
  2. 2
    Otrowas partitioned between EtOAc/H2O (3×)
  3. 3
    Lavadothe combined organics were washed with satd
  4. 4
    Secadoaq. NaCl, dried over Na2SO4
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated
  7. 7
    OtroThe crude residue was purified by chromatography (SiO2, 0-15% EtOAc/toluene)

Procedimiento

3,6-Dibromocarbazole (0.500 g, 1.538 mmol), NaN3 (0.120 g, 1.846 mmol), CuI (0.029 g, 0.154 mmol), L-proline (0.053 g, 0.461 mmol) and NaOH (0.019 g, 0.461 mmol) were dissolved in 7:3 EtOH/H2O (3.0 mL) and heated to 95° C. under a N2 atmosphere for 24 h. The completed reaction was partitioned between EtOAc/H2O (3×) and the combined organics were washed with satd. aq. NaCl, dried over Na2SO4, filtered, and concentrated. The crude residue was purified by chromatography (SiO2, 0-15% EtOAc/toluene), followed by HPLC (Phenomenex SiO2 Luna 10μ, 250×21.2 mm column, 50% EtOAc/Hexane, 21 mL/min, retention time=48 min) to afford the desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09095572B2uspto-grants-2015_08