反応式
[ClH:1].[F:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][N:14]([C:17]([C:19]3[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[CH:22]=[CH:21][N:20]=3)=[O:18])[CH2:13][CH2:12]2)=[CH:5][CH:4]=1>CC(C)=O.CCOCC>[ClH:1].[F:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][N:14]([C:17]([C:19]3[C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[CH:22]=[CH:21][N:20]=3)=[O:18])[CH2:13][CH2:12]2)=[CH:5][CH:4]=1参加物
5
実験手順
For salt formation, 1N hydrochloric acid is added to a solution of {4-[2-(4-fluorophenyl)ethyl]piperazin-1-yl}isoquinolin-1-ylmethanone in 60 ml of acetone and 50 ml of ether until crystals form. When crystallisation is complete, the mother liquor is filtered off, and the precipitate is washed with ether and dried, giving {4-[2-(4-fluorophenyl)ethyl]piperazin-1-yl}isoquinolin-1-ylmethanone, hydrochloride, m.p. 238-240°.
後処理
- customform
- customWhen crystallisation
- filtrationthe mother liquor is filtered off
- washthe precipitate is washed with ether
- customdried
出典と根拠
- ORDレコード
- ord-d0a23f68871b41f4a282286bf96a4ab9
- 出典データセット
- uspto-grants-2008_02
- 特許番号
- US07329749B2
関連ノート
読み込み中…