Reacción #1244271

ord-9b99331a26a94464b68b74bc370e9dda

Ecuación de reacción

C#CCNC(=O)CBr
alkyne
C#CCNC(=O)CBr
2-Bromo-N-(prop-2-ynyl)acetamide
C#CCn1ccnc1[N+](=O)[O-]
2-nitroimidazole
C#CCn1ccnc1[N+](=O)[O-]
2-Nitro-1-(prop-2-ynyl)-1H-imidazole
O=C([O-])[O-].[K+].[K+]
K2CO3
C#CCNC(=O)Cn1ccnc1[N+](=O)[O-]
white solid
Rendimiento 18.0%
C#CCNC(=O)Cn1ccnc1[N+](=O)[O-]
2-(2-Nitro-1H-imidazol-1-yl)-N-(prop-2-ynyl)acetamide
Rendimiento 18.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe resultant precipitate (1.2 g) was filtered off
  2. 2
    Lavadowashed with water (2×40 mL)
  3. 3
    ExtracciónThe aqueous layer was extracted into EtOAc
  4. 4
    ConcentraciónThe organic layer was concentrated to dryness
  5. 5
    OtroThe material was purified on a silica gel cartridge

Procedimiento

To a round bottom flask was added alkyne 18 (1.56 g, 8.84 mmol), 2-nitroimidazole 10 (1 g, 8.84 mmol) and K2CO3 (1.22 g, 8.84 mmol) in DMF (10 mL). The reaction was stirred overnight. The reaction was diluted with water (100 mL) and the resultant precipitate (1.2 g) was filtered off and washed with water (2×40 mL). The aqueous layer was extracted into EtOAc. The organic layer was concentrated to dryness and combined with the precipitate. The material was purified on a silica gel cartridge using EtOAc:Hex as the eluent to afford a 19 white solid (324 mg, 18%). Mass Spec (lo-res): Calc'd for C8H8N4O3: 208.06; found: 209.10 (M+H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07807394B2uspto-grants-2010_10