Acetic Acid → 8-(3-morpholin-4-yl-prop-1-ynyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylate
反応式
C=O.[NH:3]1[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[C:9]([C:11]1[CH:20]=[CH:19][C:18]2[NH:17][C:16](=[O:21])[C:15]3[NH:22][CH:23]=[CH:24][C:14]=3[C:13]=2[CH:12]=1)#[CH:10].[CH2:25]([C:27]([O-:29])=[O:28])[CH3:26].C(O)(=O)C>O1CCOCC1.[Cu](I)I>[N:3]1([CH2:25][C:10]#[C:9][C:11]2[CH:20]=[CH:19][C:18]3[NH:17][C:16](=[O:21])[C:15]4[NH:22][CH:23]=[CH:24][C:14]=4[C:13]=3[CH:12]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[CH2:25]([C:27]([O-:29])=[O:28])[CH3:26]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 85 °C
実験手順
15 mg (0.17 mmol) of para-formaldehyde, 15 mg (0.17 mmol) of morpholine and 3 mg (0.02 mmol) of copper iodide are added to a suspension of 47 mg (0.17 mmol) of 8-ethynyl-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in 5 ml of anhydrous dioxan, then a drop of acetic acid is added and the mixture is heated at 85° C. for 48 hours. The raw reaction product is then filtered, the filtrate is evaporated and the residue is purified by preparative LCMS to give 4 mg (6%) of 8-(3-morpholin-4-yl-prop-1-ynyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in the form of a white solid.
後処理
- customThe raw reaction product
- filtrationis then filtered
- customthe filtrate is evaporated
- customthe residue is purified by preparative LCMS
出典と根拠
- ORDレコード
- ord-8238585474ac455e8dddcc24e92d73f8
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08426437B2
反応ノート
読み込み中…