Réaction #47703

ord-e3890998a6f74fe4bce322bc689e3077

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction mixtures
  2. 2
    Autreto precipitate the dye
  3. 3
    FiltrationThe precipitate was filtered off
  4. 4
    Lavagewashed with 3 times with 25 ml of ethyl acetate
  5. 5
    Autrebefore being dried under vacuum until a constant weight
  6. 6
    Autrewas obtained
  7. 7
    Autre1.09 g of orange powder were recovered

Mode opératoire

0.800 g of N,N-diethyl-2-(3-formyl-1H-indol-1-yl)acetamide was solubilized in 4.2 ml of isopropanol. 0.238 g of piperidine was added, followed by 0.435 g of 2,3-dihydro-1H-indolizinium chloride dissolved in 7 ml of isopropanol. The reaction mixtures were brought to 80° C. for 24 h, with stirring. 50 ml of ethyl acetate were added in order to precipitate the dye. The precipitate was filtered off, and washed with 3 times with 25 ml of ethyl acetate before being dried under vacuum until a constant weight was obtained. 1.09 g of orange powder were recovered. The analyses were in conformity with the expected structure.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07744658B2uspto-grants-2010_06