反応 #7696
ord-28046646c1654096b7755cc2c17642b7
反応方程式
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他Then 4 ml of the reaction mixture was separated
- 2その他quenched with MeOH
- 3その他After solvents were removed under vaccum
- 4その他the residue was purified
実験手順
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).