Reacción #1543814

ord-b14ad014430f47b1942513e31bab5ec2

Ecuación de reacción

[N-]=[N+]=NC1CCc2ccccc2NC1=O
3-azido-2,3,4,5-tetrahydro-1H-[1]-benzazapin-2-one
[N-]=[N+]=NC1CCc2ccccc2NC1=O
3-Azido-2,3,4,5-tetrahydro-1H-[1]-benzazapin-2-one
NC1CCc2ccccc2NC1=O
3-Amino-2,3,4,5-tetrahydro-1H-[1]-benzazapin-2-one

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe flask was purged with nitrogen
  2. 2
    workup.ADDITIONcharged with 55 psig hydrogen
  3. 3
    Filtraciónfiltered through celite
  4. 4
    Concentraciónconcentrated
  5. 5
    OtroThe residue was recrystallized from MEOH
  6. 6
    Otroto give 6.77 g (78%) in two crops

Procedimiento

To a suspension of 10.0 g (49.4 mmol) of 3-azido-2,3,4,5-tetrahydro-1H-[1]-benzazapin-2-one (Example 3 above) in 100 mL of methanol/ethanol (1:1) was added 1 g of 10% palladium on charcoal and the flask was purged with nitrogen and charged with 55 psig hydrogen. The mixture was shaken for 5 h, filtered through celite and concentrated. The residue was recrystallized from MEOH to give 6.77 g (78%) in two crops. 1H NMR (300 MHz, CDCl3) d 8.38 (1H, bs), 7.3-7.1 (3H, m), 6.98 (1H, d, J=8 Hz), 3.42 (1H, dd, J=11, 7 Hz), 2.90 (1H, m), 2.70-2.40 (2H, m), 1.89 (1H, m), 1.78 (bs, 2H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05843941uspto-grants-1998_12