Reaktion #159376

ord-0875dc4f41854179839123d1593d5957

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08828991B2uspto-grants-2014_09