Réaction #2028881

ord-90e1733e1b94481ebc7bb8f99b8044b9

Équation de réaction

NS(=O)(=O)c1ccc(-n2nc(CO)cc2-c2ccccc2)cc1
alcohol
NS(=O)(=O)c1ccc(-n2nc(CO)cc2-c2ccccc2)cc1
4-[3-hydroxymethyl-5-phenyl-1H-pyrazol-1-yl]benzene Sulfonamide
NS(=O)(=O)c1ccc(-n2nc(C=O)cc2-c2ccccc2)cc1
aldehyde
NS(=O)(=O)c1ccc(-n2nc(C=O)cc2-c2ccccc2)cc1
4-[3-formyl-5-phenyl-1H-pyrazol-1-yl]benzenesulfonamide

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe mixture was filtered through Celite
  2. 2
    Concentrationthe solution was concentrated

Mode opératoire

To a solution of the alcohol prepared in Example 131, Step 3 (1.1 g, 3.3 mmol) in ethyl acetate (20 mL) was added MnO2 (5 g, 60 mmol) and the mixture stirred at room temperature overnight. The mixture was filtered through Celite and the solution was concentrated to provide the crude aldehyde.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE044048E1uspto-grants-2013_03