Реакция #7695

ord-a40547b8595849ebabaf584db239ee95

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другое4 ml of solution was separated
  2. 2
    Другоеquenched with MeOH
  3. 3
    ДругоеAfter solvents were removed under vaccum
  4. 4
    Другоеthe residue was purified

Методика

NaHMDS (1.48 ml, 1M in THF) was added into a solution of (R)-N-benzoyl-3-methyl-N′-(2-cyano-acetyl)piperazine (190 mg) and 2-chlorobenzothiazole (100 mg) in THF (10 ml). After the reaction was stirred for 10 hours, 4 ml of solution 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′-[(benzothiazol-2-yl)-2-cyanoacetyl]-piperazine (15.4 mg).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07087610B2uspto-grants-2006_08