反応式
O.O.[C:3]([OH:8])(=[O:7])[C:4]([OH:6])=[O:5].[CH3:9][N:10]([CH2:12][CH2:13][CH2:14][C@@:15]1([C:26]2[CH:27]=[CH:28][C:29]([F:32])=[CH:30][CH:31]=2)[O:23][CH2:22][C:21]2[CH:20]=[C:19]([C:24]#[N:25])[CH:18]=[CH:17][C:16]1=2)[CH3:11]>CC(O)C>[CH3:9][N:10]([CH2:12][CH2:13][CH2:14][C@@:15]1([C:26]2[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=2)[O:23][CH2:22][C:21]2[CH:20]=[C:19]([C:24]#[N:25])[CH:18]=[CH:17][C:16]1=2)[CH3:11].[C:4]([OH:6])([C:3]([OH:8])=[O:7])=[O:5]参加物
4
反応条件
- 温度
- 40 °C
実験手順
100 g of the free base was dissolved in 250 mL of 2-propanol. 1 eq. of oxalic acid dihydrate was dissolved in 250 mL of warm 2-propanol and was added at 40° C. to the solution of escitalopram base. After stirring at 40° C. for 10 min the crystallization started. The mixture was then allowed to cool to room temperature and stirred for ca. 2 hours. The crystals were filtered off, rinsed on the filter with 2-propanol and dried to constant weight under vacuum at 60° C.
後処理
- customthe crystallization
- temperatureto cool to room temperature
- stirringstirred for ca. 2 hours
- filtrationThe crystals were filtered off
- washrinsed on the
- filtrationfilter with 2-propanol
- customdried to constant weight under vacuum at 60° C.
出典と根拠
- ORDレコード
- ord-57ef3879331d4015967fe79978f9764d
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07560576B2
関連ノート
読み込み中…