Iodoethane → 4,4-Dimethyl-1-ethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarbonitrile
反応式
[CH3:1][C:2]1([CH3:18])[C:11]2[C:6](=[CH:7][C:8]([C:12](O)=O)=[CH:9][CH:10]=2)[N:5]([CH2:15][CH3:16])[C:4](=[O:17])[CH2:3]1.CC1(C)C2C(=CC(C(O)=O)=CC=2)[NH:23]C(=O)C1.CC1(C)C2C(=CC(C#N)=CC=2)NC(=O)C1.ICC.C(=O)([O-])[O-].[K+].[K+]>O>[CH3:1][C:2]1([CH3:18])[C:11]2[C:6](=[CH:7][C:8]([C:12]#[N:23])=[CH:9][CH:10]=2)[N:5]([CH2:15][CH3:16])[C:4](=[O:17])[CH2:3]1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
One prepared 4,4-dimethyl-1-ethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarboxylic acid analogously to the procedure for 4,4-dimethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarboxylic acid (DE-A-3,818,830) as follows: one stirred 4,4-dimethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarbonitrile (2.0 g, 10.0 mmol), iodoethane (1 ml, 12.0 mmol) and potassium carbonate (1.70 g, 12.0 mmol) for one hour at 60° C., again added iodoethane (2 ml, 24 mmol) and potassium carbonate (2.5 g, 25 mmol) thereto and stirred for one hour at 60° C. One allowed to cool to room temperature, stirred the solution into water, filtered off the precipitate with suction and dried in a vacuum. One obtains 4,4-dimethyl-1-ethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarbonitrile (1.1 g, 48%) with the m.p.=120°-121° C.
後処理
- filtrationfiltered off the precipitate with suction
- customdried in a vacuum
出典と根拠
- ORDレコード
- ord-0ff424f5b43a4079bc237d94d0b98811
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05414088
反応ノート
読み込み中…