Reaktion #6961

ord-4b2bf3783bd943be8a72c6dd87d5cd4d

Reaktionsgleichung

CN
methylamine
Nc1cc(C(=O)O)c(F)cc1F
2,4-difluoro-5-aminobenzoic acid
CCN=C=NCCCN(C)C
EDCI
On1nnc2ccccc21
HOBt
CNC(=O)c1cc(N)c(F)cc1F
5-amino-2,4-difluoro-N-methylbenzamide
Ausbeute 41.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat RT
  2. 2
    Waschenwashed with water (100 mL)
  3. 3
    ExtraktionThe aqueous layer was extracted with ethyl acetate (2×50 mL)
  4. 4
    WaschenThe combined organic layer was washed with NaHCO3 (3×50 mL)
  5. 5
    SonstigeThe organic layer was dried
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated

Vorschrift

To a solution of 2,4-difluoro-5-aminobenzoic acid (1.73 g, 10.0 mmol) in DMF (40 mL) were successively added EDCI (1.62 g, 12.0 mmol), HOBt (2.30 g, 12.0 mmol) and methylamine (6.0 mL, 12.0 mmol, 2 M in MeOH) in that order at RT. After stirring for 2 h, the reaction mixture was diluted with ethyl acetate (100 mL) and washed with water (100 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layer was washed with NaHCO3 (3×50 mL) followed by 10% LiCl (50 mL). The organic layer was dried, filtered and concentrated to afford 5-amino-2,4-difluoro-N-methylbenzamide (0.76 g, 41%) as a light brownish solid. MS (M+H)+=187. It was used without further purification (>92% pure by HPLC).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084160B2uspto-grants-2006_08