Reaktion #43759

ord-77a62f0e4b7944e3b6ec94e968bf016a

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture is purified by preparative HPLC
  2. 2
    EinengenThe product fractions are concentrated
  3. 3
    workup.DISSOLUTIONdissolved in a mixture of methanol and 4M HCl in dioxane
  4. 4
    Einengenagain concentrated
  5. 5
    Sonstigedried under high vacuum

Vorschrift

83 mg (0.23 mmol) of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-3-chloro-6-nitro-1-benzothiophene-2-carboxamide hydrochloride are dissolved in 1.5 ml of 2M tin(II) chloride solution in DMF and stirred at RT for 14 h. The reaction mixture is purified by preparative HPLC. The product fractions are concentrated, dissolved in a mixture of methanol and 4M HCl in dioxane, then again concentrated and dried under high vacuum. 53 mg (57.2% of theory) of the title compound are obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732477B2uspto-grants-2010_06