Reacción #48897

ord-c883adedf8324d22b12958b209992724

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux for 15 min
  2. 2
    workup.ADDITIONThe obtained precipitate (mixture of the diastereomers
  3. 3
    Extracciónand OB-5.5b) was extracted by suction
  4. 4
    Lavadowashed with ether
  5. 5
    Otrodried

Procedimiento

642 mg (1 mmol) 3-methyl-2-((1E,3E)-4-phenylamino-buta-1,3-dienyl)-5-sulfo-1,3-bis-(3-sulfo-propyl)-3H-indolium disodium salt and 483 mg (1 mmol) 3-(3-Carboxypropyl)-2,3-dimethyl-5-sulfonato-1-(3-sulfopropyl)-3H-indolium sodium salt were dissolved in a mixture of 10 ml acetic acid and 10 ml acetic anhydride. Five ml pyridine was added. The solution was stirred under reflux for 15 min. Twenty ml ether was added after cooling to room temperature. The obtained precipitate (mixture of the diastereomers OB-5.5a and OB-5.5b) was extracted by suction, washed with ether, and dried.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745640B2uspto-grants-2010_06