1,4-Dioxane hydrochloride → 1-(2-Fluoro-3-(trifluoromethyl)benzoyl)piperazine hydrochloride
反応式
[F:1][C:2]1[C:22]([C:23]([F:26])([F:25])[F:24])=[CH:21][CH:20]=[CH:19][C:3]=1[C:4]([N:6]1[CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8][CH2:7]1)=[O:5].[ClH:27].O1CCOCC1>CO>[ClH:27].[F:1][C:2]1[C:22]([C:23]([F:26])([F:24])[F:25])=[CH:21][CH:20]=[CH:19][C:3]=1[C:4]([N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5]参加物
4
実験手順
To a mixture of 7.74 g of tert-butyl 4-(2-fluoro-3-(trifluoromethyl)benzoyl)piperazine-1-carboxylate and 10 ml of methanol was added a hydrochloric acid-1,4-dioxane solution (4 M, 20 ml) followed by stirring at room temperature for 4 hours. The reaction mixture was concentrated in vacuo to give the title compound.
後処理
- concentrationThe reaction mixture was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-3226fcc81deb4e769210b241a4538192
- 出典データセット
- uspto-grants-2010_11
- 特許番号
- US07834018B2
反応ノート
読み込み中…