Reacción #6757

ord-7b901fc15a6e4f8abc6c1204b5292bcc

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction mixture was concentrated under reduced pressure, and diethyl ether
  2. 2
    workup.ADDITIONwas added to the residue
  3. 3
    OtroThe resulting precipitated crystal
  4. 4
    Filtraciónwas collected by filtration

Procedimiento

To a solution of 4-[(4-ethylthiophenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methyl-1H-pyrazole (0.41 g) in tetrahydrofuran (10 mL) were added acetic acid (0.11 mL) and acetic anhydride (0.18 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and diethyl ether was added to the residue. The resulting precipitated crystal was collected by filtration to give 1-acetyl-4-[(4-ethylthiophenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methylpyrazole (0.36 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084123B2uspto-grants-2006_08