Acetic Acid → Methyl 5-cyano-4-(5-fluoro-2-methyl-4-oxo-4H-chromen-8-yl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylate
反応式
[F:1][C:2]1[CH:11]=[CH:10][C:9]([CH:12]=O)=[C:8]2[C:3]=1[C:4](=[O:15])[CH:5]=[C:6]([CH3:14])[O:7]2.[C:16]([CH:18]=[C:19]([O-])[CH3:20])#[N:17].[Na+].[NH2:23]/[C:24](/[CH3:30])=[CH:25]\[C:26]([O:28][CH3:29])=[O:27].C(O)(=O)C>CC(O)C>[C:16]([C:18]1[CH:12]([C:9]2[CH:10]=[CH:11][C:2]([F:1])=[C:3]3[C:8]=2[O:7][C:6]([CH3:14])=[CH:5][C:4]3=[O:15])[C:25]([C:26]([O:28][CH3:29])=[O:27])=[C:24]([CH3:30])[NH:23][C:19]=1[CH3:20])#[N:17]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of 100 mg (0.49 mmol) of 5-fluoro-2-methyl-4-oxo-4H-chromene-8-carbaldehyde in 5 ml of 2-propanol is mixed with 50.96 mg (0.49 mmol) of sodium 1-cyanoprop-1-en-2-olate, 55.84 mg (0.49 mmol) of methyl 3-aminocrotonate and 0.04 ml (0.73 mmol) of acetic acid and stirred under reflux for 3 h. After cooling, the mixture is concentrated. The residue is taken up in dichloromethane and washed with water. The organic phase is dried over sodium sulfate and concentrated. The resulting residue is crystallized from diethyl ether. The beige-colored crystals are filtered off with suction and dried at 40° C. in a vacuum drying oven. 128.3 mg (71.8% of theory) of the title compound are obtained.
後処理
- temperatureunder reflux for 3 h
- temperatureAfter cooling
- concentrationthe mixture is concentrated
- washwashed with water
- dry with materialThe organic phase is dried over sodium sulfate
- concentrationconcentrated
- customThe resulting residue is crystallized from diethyl ether
- filtrationThe beige-colored crystals are filtered off with suction
- customdried at 40° C. in a vacuum
- customdrying oven
出典と根拠
- ORDレコード
- ord-45f146c5cbcc426fa4b5f387e35ae19d
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08058447B2
反応ノート
読み込み中…