Reaktion #43862

ord-d8e75d7e77ea44ca9dac7480559a22da

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered through an Extrelut column
  2. 2
    WaschenThe Extrelut column was washed with CH2Cl2
  3. 3
    Einengenthe filtrate was concentrated

Vorschrift

Cyclopentanecarbonyl chloride (43 μL, 0.36 mmol) was added to a solution of (5-benzylamino-2-propyl-benzoimidazol-1-yl)-acetic acid tert-butyl ester (45 mg, 0.12 mmol), DIEA (41 μL, 0.24 mmol) and DMAP (15 mg, 0.12 mmol) in CH2Cl2 (1 mL), and stirred overnight at room temperature. The reaction solution was diluted with aqueous HCl (1.0 M) and filtered through an Extrelut column. The Extrelut column was washed with CH2Cl2, and the filtrate was concentrated to afford the subtitle compound that was used without further purification. MS calculated for C29H37N3O3+H: 476, observed: 476.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732618B2uspto-grants-2010_06