反応 #2460332

ord-6237dd45be50410bb32ecfa836607e1d

反応方程式

Cc1cc2c(s1)Nc1ccccc1N=C2N1CCN(C)CC1
olanzapine
Cc1cc2c(s1)Nc1ccccc1N=C2N1CCN(C)CC1
olanzapine
O=C(O)c1ccccc1
benzoic acid
O=C(O)c1ccccc1
benzoic acid
Cc1cc2c(s1)=Nc1ccccc1NC=2N1CCN(C)CC1.O=C(O)c1ccccc1
Olanzapine Benzoate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他(T=50-55° C.)
  2. 2
    workup.STIRRINGwhile stirring
  3. 3
    その他The pale yellow crystals were isolated by filtration
  4. 4
    その他dried overnight at 40° C. in vacuum
  5. 5
    その他Isolated yield: 130.1 gram (94%)
  6. 6
    その他at 222.99° C.

実験手順

To a clear solution (50° C.) of 100 g olanzapine free base in 2000 ml ethyl acetate, was added slowly a clear solution of 39.2 g benzoic acid in 250 ml ethyl acetate while stirring mechanically. When almost all benzoic acid was added, the crystallization process started (T=50-55° C.). The mixture was allowed to cool to room temperature while stirring. The pale yellow crystals were isolated by filtration and dried overnight at 40° C. in vacuum. Isolated yield: 130.1 gram (94%). 1H-NMR confirms the molar ratio of olanzapine:acid=1:1. DSC: peak at 222.99° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07459449B2uspto-grants-2008_12