Hydrochloric Acid → 7-(4-ethoxyphenyl)-N-[4-[N-methyl-N-(4-oxocyclohexyl)aminomethyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide
反応式
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[S:19](=[O:21])(=[O:20])[CH2:18][CH2:17][C:16]([C:22]([NH:24][C:25]4[CH:30]=[CH:29][C:28]([CH2:31][N:32]([CH:34]5[CH2:39][CH2:38][C:37]6(OCC[O:40]6)[CH2:36][CH2:35]5)[CH3:33])=[CH:27][CH:26]=4)=[O:23])=[CH:15][C:14]=3[CH:44]=2)=[CH:6][CH:5]=1)[CH3:2].Cl.C(=O)(O)[O-].[Na+]>C1COCC1>[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:11]=[CH:12][C:13]3[S:19](=[O:21])(=[O:20])[CH2:18][CH2:17][C:16]([C:22]([NH:24][C:25]4[CH:26]=[CH:27][C:28]([CH2:31][N:32]([CH3:33])[CH:34]5[CH2:39][CH2:38][C:37](=[O:40])[CH2:36][CH2:35]5)=[CH:29][CH:30]=4)=[O:23])=[CH:15][C:14]=3[CH:44]=2)=[CH:6][CH:5]=1)[CH3:2]参加物
実験手順
To a solution of 7-(4-ethoxyphenyl)-N-[4-[N-(4,4-ethylenedioxycyclohexyl)-N-methylaminomethyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide (140 mg) in THF (20 ml) was added at room temperature 3N hydrochloric acid (1 ml), and the mixture was stirred for 40 hours. To the mixture was added saturated sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried with magnesium sulfate and concentrated under reduced pressure to give colorless solid, which was recrystallized from ethyl acetate/hexane to give colorless crystals of 7-(4-ethoxyphenyl)-N-[4-[N-methyl-N-(4-oxocyclohexyl)aminomethyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide (Compound 19) (101.1 mg).
後処理
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with saturated brine
- dry with materialdried with magnesium sulfate
- concentrationconcentrated under reduced pressure
- customto give colorless solid, which
- customwas recrystallized from ethyl acetate/hexane
出典と根拠
- ORDレコード
- ord-95fe5b75bec341a193b03d81d3f9faba
- 出典データセット
- uspto-grants-2001_05
- 特許番号
- US06235771B1
反応ノート
読み込み中…