Reaktion #730196

ord-06a96cf62b654737b41d01dea72ffdae

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenconcentrated in vacuo
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in 1 mL and 5 mL DMSO

Vorschrift

5-Chloro-N-((1-(4-(3-methoxy-2-oxopyridin-1(2H)-yl)phenyl)-1H-1,2,3-triazol-4-yl)methyl)thiophene-2-carboxamide (306 mg, 0.69 mmol, prepared using a similar procedure as described in Example 4) was stirred in 40 mL DCM as a slurry. BBr3 (200 μL, 2.1 mmol) was added. The mixture was stirred for 2 hrs and concentrated in vacuo. The residue was dissolved in 1 mL and 5 mL DMSO and subjected to prep HPLC to isolate the title compound as a white powder. MS found for C19H14ClN5O3S (M+H)+ 428.1, 430.1 (Cl pattern).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07696352B2uspto-grants-2010_04