Reaktion #7696

ord-28046646c1654096b7755cc2c17642b7

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThen 4 ml of the reaction mixture was separated
  2. 2
    Sonstigequenched with MeOH
  3. 3
    SonstigeAfter solvents were removed under vaccum
  4. 4
    Sonstigethe residue was purified

Vorschrift

NaHMDS (0.77 ml, 1M in THF) was added into a solution of (R)-N-benzyl-3-methyl-N′-cyanomethylpiperazine (100 mg) and 2-cyano-5-methoxy-benzothiazole (58 mg) in THF (10 ml). The reaction was stirred for 10 hours. Then 4 ml of the reaction mixture was separated and quenched with MeOH. After solvents were removed under vaccum, the residue was purified using Shimadzu automated preparative HPLC System to give (R)-N-(benzoyl)-3-methyl-N′-[2-(5-methoxy-benzothiazol-2-yl)-2-imino-1-cyano-ethyl]-piperazine (1.3 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087610B2uspto-grants-2006_08