Reacción #92032

ord-ce9c8c2a793b4da39941669816888f57

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe resulting reaction mixture
  2. 2
    Lavadowashed three times with water and one time with brine
  3. 3
    SecadoThe extract was dried over anhydrous sodium sulfate
  4. 4
    Concentraciónconcentrated under reduced pressure
  5. 5
    workup.DISSOLUTIONredissolved in small amount of methanol and ethyl acetate
  6. 6
    Otrotriturated with diethyl ether

Procedimiento

Cystamine dihydrochloride (68 mg, 0.301 mmol) and DIEA (110 μL, 2.1 eq.) were dissolved in DMF (10 mL), followed by addition of NHS-fluorescein, a mixture of 5- and 6-carboxyfluorescein (300 mg, 0.634 mmol) and the resulting reaction mixture was stirred overnight at room temperature. Then it was diluted with ethyl acetate and washed three times with water and one time with brine. The extract was dried over anhydrous sodium sulfate, concentrated under reduced pressure, redissolved in small amount of methanol and ethyl acetate, and then triturated with diethyl ether to obtain 140 mg of fluorescein-cystamine adduct as a bright orange solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09447035B2uspto-grants-2016_09