Reaktion #2481500

ord-c7321aa1db03415f998b49215826b69d

Reaktionsgleichung

Cl
Hydrogen chloride
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C.N#N
N2 tert-butoxycarbonyl-N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](N)C(C)C.Cl
desired product
Ausbeute 100.0%
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](N)C(C)C.Cl
N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide hydrochloride
Ausbeute 100.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter the completion of the reaction
  2. 2
    Sonstigethe methylene chloride was removed under reduced pressure
  3. 3
    Sonstigethus yielding a crude crystal
  4. 4
    WaschenThe crude crystal was washed with acetone

Vorschrift

Hydrogen chloride gas was introduced into a solution containing 3.7 g of N2 -tert-butoxycarbonyl-N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide dissolved in 100 ml of methylene chloride for 1 hour at room temperature. After the completion of the reaction, the methylene chloride was removed under reduced pressure, thus yielding a crude crystal. The crude crystal was washed with acetone to afford 3.1 g of the desired product (yield: 100%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05811424uspto-grants-1998_09