Reaktion #93166

ord-00f2f8924f234895ae8b88ec613b5bd8

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent removed at reduced pressure
  2. 2
    Filtrationthe solid product collected by filtration
  3. 3
    workup.DISSOLUTIONThe product was dissolved in methanol
  4. 4
    workup.ADDITIONacetonitrile added

Vorschrift

1-[5-Methoxy-2-(4-pyridinylamino)benzoyl]piperidine (Example 30b) (9.2 g) was dissolved in 100 ml of methylene dichloride. To this solution was added dropwise 80 ml of boron tribromide solution (0.8M in methylene dichloride). The mixture was kept at room temperature overnight and the solvent removed at reduced pressure. The residue was made basic with aqueous potassium carbonate and the solid product collected by filtration. The product was dissolved in methanol and acetonitrile added to produce 4.9 g of 1-[5-hydroxy-2-(4-pyridinylamino)benzoyl]piperidine. A further recrystallization from methanol gave a sample with m.p. 242°-243° C.(decompn.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04610991uspto-grants-1986_09