Hydrogen chloride-ethyl acetate → 2-(4-carboxybenzyl)-6-dimethylcarbamoyl-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl Ester
反応式
C(OC(=O)C)C.Cl.[CH3:8][O:9][C:10]([C:12]1[N:13]([CH2:34][C:35]2[CH:40]=[CH:39][C:38]([C:41]([O:43]C(C)(C)C)=[O:42])=[CH:37][CH:36]=2)[C:14](=[O:33])[C:15]2[C:20]([C:21]=1[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[CH:19][C:18]([C:28](=[O:32])[N:29]([CH3:31])[CH3:30])=[CH:17][CH:16]=2)=[O:11]>>[CH3:8][O:9][C:10]([C:12]1[N:13]([CH2:34][C:35]2[CH:36]=[CH:37][C:38]([C:41]([OH:43])=[O:42])=[CH:39][CH:40]=2)[C:14](=[O:33])[C:15]2[C:20]([C:21]=1[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)=[CH:19][C:18]([C:28](=[O:32])[N:29]([CH3:30])[CH3:31])=[CH:17][CH:16]=2)=[O:11]参加物
3
反応物 2
生成物 1
実験手順
To a 4N-hydrochloric acid ethyl acetate solution (4 ml) was added 2-(4-tert-butoxycarbonylbenzyl)-6-dimethylcarbamoyl-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester (140 mg), and the mixture was stirred at room temperature for 4 hrs. The reaction mixture was concentrated under reduced pressure, and the obtained residue was crystallized from methanol-diisopropyl ether to give the title compound (86 mg).
後処理
- concentrationThe reaction mixture was concentrated under reduced pressure
- customthe obtained residue was crystallized from methanol-diisopropyl ether
出典と根拠
- ORDレコード
- ord-ad8dcc0bdc6f40cbb3234a96ac85daf0
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07402595B2
反応ノート
読み込み中…