Reaktion #738695

ord-1f7c8983d0d047c3a0c25bb6e24d80d2

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed in vacuo
  2. 2
    Sonstigethe residue was purified by flash column chromatography (10% methanol in methylene chloride saturated with. NH3)

Vorschrift

2-Chlorobenzenesulfonic acid 3[[N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]-5-methylphenyl ester (745 mg, 1.5 mmol), as prepared in the preceding step, was treated with 4 N HCl in 1,4-dioxane (20 mL) at room temperature for 2 H. The solvent was removed in vacuo and the residue was purified by flash column chromatography (10% methanol in methylene chloride saturated with. NH3) to give the title compound as a colorless syrup (570 mg 95%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06281206B1uspto-grants-2001_08