Reaktion #43764

ord-dbe54efce1fc46abbe9ff71c0e0b13e9

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture is purified by preparative HPLC
  2. 2
    workup.DISSOLUTIONThe product is dissolved in a mixture of 1N aqueous hydrochloric acid and acetonitrile
  3. 3
    Sonstigedried under high vacuum

Vorschrift

40 mg (0.11 mmol) of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-amino-1-benzo-thiophene-2-carboxamide hydrochloride are dissolved in 2 ml of DMF, 6.5 mg (0.05 mmol) of N,N-dimethyl-4-aminopyridine, 59.6 μl (0.43 mmol) of triethylamine and 16.61 (0.21 mmol) of methanesulfonyl chloride are added and the mixture is stirred at room temperature for 16 h. The reaction mixture is purified by preparative HPLC. The product is dissolved in a mixture of 1N aqueous hydrochloric acid and acetonitrile, then reconcentrated and dried under high vacuum. 15 mg (33.8% of theory) of the title compound are obtained.

Quelle

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