Reacción #996520

ord-997f33c6696e45bb8bf69416cb9f84e3

Disolventes

Condiciones de reacción

Temperatura
5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGAfter stirring for 16 hours
  2. 2
    Otrothe layers were separated
  3. 3
    Extracciónthe aqueous fraction was extracted with chloroform
  4. 4
    LavadoThe combined organic fractions were sequentially washed with 5% aqueous sodium bicarbonate, water and brine
  5. 5
    Secadodried over anhydrous sodium sulfate
  6. 6
    Filtraciónfiltered
  7. 7
    Concentraciónconcentrated under reduced pressure
  8. 8
    OtroThe residue was purified by flash column chromatography on silica gel
  9. 9
    OtroThe purification
  10. 10
    Lavadowas carried out eluting with chloroform
  11. 11
    OtroThe material recovered from the column
  12. 12
    Otrowas recrystallized from acetonitrile

Procedimiento

7-Bromo-2-ethoxymethyl-1-(3-isopropoxypropyl)-1H-imidazo[4,5-c]quinoline (20 g) was dissolved in chloroform (400 mL). 3-Chloroperoxybenzoic acid (60% pure, 17.1 g) was added in 2 g portions over a 5 minute period and the reaction was stirred for 1 hour. Ammonium hydroxide (300 mL) was added and the mixture was cooled to 5° C. with an ice/water bath. p-Toluenesulfonyl chloride (9.4 g) was added at the rate of 1 g/min to minimize gas evolution. After stirring for 16 hours, the layers were separated and the aqueous fraction was extracted with chloroform. The combined organic fractions were sequentially washed with 5% aqueous sodium bicarbonate, water and brine; dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel. The polar component of the eluent was chloroform:methanol:ammonium hydroxide 80:18:2 (CMA). The purification was carried out eluting with chloroform:CMA in a gradient from 98:2 to 88:12. The material recovered from the column was recrystallized from acetonitrile to yield 7.0 g of 7-bromo-2-ethoxymethyl-1-(3-isopropoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine as a tan granular powder.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08017779B2uspto-grants-2011_09