Reacción #159376

ord-0875dc4f41854179839123d1593d5957

Ecuación de reacción

Cc1cc(F)ccc1[N+](=O)[O-]
4-fluoro-2-methyl-1-nitrobenzene
CN(C)C1CCNC1
dimethylpyrrolidin-3-ylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cc(N2CCC(N(C)C)C2)ccc1[N+](=O)[O-]
Dimethyl-[1-(3-methyl-4-nitrophenyl)pyrrolidin-3-yl]amine

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was partitioned between water and ethyl acetate
  2. 2
    OtroThe organic phase was dried
  3. 3
    Concentraciónconcentrated
  4. 4
    OtroThe product with the molecular weight of 249.32 (C13H19N3O2) was obtained in this way

Procedimiento

A mixture of 4-fluoro-2-methyl-1-nitrobenzene (13.6 g), dimethylpyrrolidin-3-ylamine (10.0 g), potassium carbonate (12 g) and DMF (100 mL) was stirred at room temperature for 4 hours. The reaction mixture was partitioned between water and ethyl acetate. The organic phase was dried and concentrated. The product with the molecular weight of 249.32 (C13H19N3O2) was obtained in this way; MS (ESI): 250 (M+H+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08828991B2uspto-grants-2014_09