Réaction #1099223

ord-ed59b666fad641eeae51fa2b47773487

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureunder reflux
  2. 2
    FiltrationThe formed precipitate was filtered
  3. 3
    Lavagewashed with ethanol
  4. 4
    Autredried in vacuum at 40° C.
  5. 5
    Autreto obtain a dark powder

Mode opératoire

3.5 g (10.33 mmol) 4-chloro-2-((E)-{4-[ethyl(2-hydroxyethyl)amino]phenyl}-diazenyl)-1,3-thiazole-5-carbaldehyde and 2.33 g (15.50 mmol) 1H-indene-1,3(2H)-dione were dissolved in 90 ml ethanole and stirred under reflux. After 6 hours the mixture was allowed to cool to room temperature. The formed precipitate was filtered, washed with ethanol and dried in vacuum at 40° C. to obtain a dark powder.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07977482B2uspto-grants-2011_07