Reaktion #1696019

ord-2039d2ca65f6416ba2cb7515b3eafa4d

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe resulting solution was concentrated until crystals
  2. 2
    Sonstigeto form
  3. 3
    TemperaturThe resulting solution was cooled
  4. 4
    Filtration2.90 g of the desired titled compound were recovered by filtration (m.p. 205°-210° C.)

Vorschrift

The titled compound was prepared substantially in accordance with the method detailed in Example 46 using 2.50 g (0.0107 mol) of 2-amino-N-[2-(1H-imidazol-2-yl)ethyl]benzamide and 4.20 g (0.0213 mol) of meta-t-butylbenzoyl chloride with the exception that, after reducing the organic layer to dryness the resulting residue was dissolved in a 1:7 methanol/ethyl acetate solution. The resulting solution was concentrated until crystals began to form and then diethyl ether was added. The resulting solution was cooled and 2.90 g of the desired titled compound were recovered by filtration (m.p. 205°-210° C.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05397798uspto-grants-1995_03