Hydrochloric Acid → (E)-3-(3-Amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile glycineamide
反応式
[NH2:1][C:2]1[CH:3]=[C:4](/[CH:10]=[C:11](\[C:14]2[CH:19]=[C:18]([O:20][CH3:21])[C:17]([O:22][CH3:23])=[C:16]([O:24][CH3:25])[CH:15]=2)/[C:12]#[N:13])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].C([NH:33][CH2:34][C:35]([NH2:37])=[O:36])(OC(C)(C)C)=O.Cl.O1CCOCC1.C(OCC)C>ClCCl>[NH2:1][C:2]1[CH:3]=[C:4](/[CH:10]=[C:11](\[C:14]2[CH:15]=[C:16]([O:24][CH3:25])[C:17]([O:22][CH3:23])=[C:18]([O:20][CH3:21])[CH:19]=2)/[C:12]#[N:13])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[NH2:33][CH2:34][C:35]([NH2:37])=[O:36]参加物
6
実験手順
Eight-hundred milligrams of (E)-3-(3-amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile-Boc-glycineamide were dissolved in 3 ml of dichloromethane, and 3 ml of a solution of 4-M hydrochloric acid and dioxane were added thereto. The mixture was reacted at room temperature for 2 hours. Thirty milliliters of diethyl ether were added thereto, and the resulting mixture was filtered. The thus-obtained powder was hot-washed with a mixture of chloroform, isopropanol and toluene at a ratio by of 6:8:20 to produce 483 mg (1.11 mmols) of the final compound in a yield of 65%.
後処理
- customThe mixture was reacted at room temperature for 2 hours
- filtrationthe resulting mixture was filtered
- washThe thus-obtained powder was hot-washed with a mixture of chloroform, isopropanol and toluene at a ratio by of 6:8:20
出典と根拠
- ORDレコード
- ord-2c28e1936d394b52b6f4aec6725f74e3
- 出典データセット
- uspto-grants-1997_10
- 特許番号
- US05674906
反応ノート
読み込み中…