Reacción #1755493

ord-5e7d845fcabf4f069a615a71f51294a8

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 65° C.
  2. 2
    Otroovernight
  3. 3
    OtroThe reaction mixture was purified by column chromatography on aminopropyl silica gel (eluent: tetrahydrofuran)
  4. 4
    OtroFurther purification by preparative thin layer chromatography on silica gel (developing solvent: ethyl acetate/hexane=2/1)

Procedimiento

To a suspension of 1,2-dihydro-4-[(4-isopropoxyphenyl)methyl]-5-methyl-3H-pyrazol-3-one (46 mg), acetobromo-α-D-glucose (99 mg) and 4 A molecular sieves in tetrahydrofuran (3 mL) was added silver carbonate (66 mg), and the mixture was stirred under shading the light at 65° C. overnight. The reaction mixture was purified by column chromatography on aminopropyl silica gel (eluent: tetrahydrofuran). Further purification by preparative thin layer chromatography on silica gel (developing solvent: ethyl acetate/hexane=2/1) afforded 4-[(4-isopropoxy-phenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole (42 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07989424B2uspto-grants-2011_08