反応式
[C:1]([CH2:3][C:4]([NH:6][C:7]1[CH:12]=[C:11]([O:13][CH3:14])[C:10]([Cl:15])=[CH:9][C:8]=1[Cl:16])=[O:5])#[N:2].[NH2:17][C:18]1[CH:19]=[CH:20][C:21]([Br:26])=[C:22]([O:24][CH3:25])[CH:23]=1.[CH2:27](OC(OCC)OCC)C>C(O)(C)C>[Br:26][C:21]1[CH:20]=[CH:19][C:18]([NH:17][CH:27]=[C:3]([C:1]#[N:2])[C:4]([NH:6][C:7]2[CH:12]=[C:11]([O:13][CH3:14])[C:10]([Cl:15])=[CH:9][C:8]=2[Cl:16])=[O:5])=[CH:23][C:22]=1[O:24][CH3:25]参加物
実験手順
To a suspension of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide (6.1 g, 23.5 mmol) in 500 mL of isopropanol was added 5-amino-2-bromoanisole (5.0 g, 24.8 mmol). This mixture was heated to reflux to give a clear yellow solution. To this solution, triethylorthoformate (10.6 mL, 63.5 mmol) was added dropwise and the reaction mixture was heated at reflux for 5 hours. An additional 10.6 mL of triethylorthoformate was added and the mixture was heated at reflux overnight. The mixture was allowed to cool to room temperature. The solid was collected by filtration, washed with isopropanol and ethyl acetate, and then dried overnight at ˜40° C. under reduced pressure to give 8.1 g (73%) of 4-bromo-3-methoxyanilino-N-(2,4-dichloro-5-methoxyphenyl)-2-cyano-2-propenamide as a yellow solid, mp >250° C.; MS (ES) m/z470.0, 472.0 (M+H)+
後処理
- temperatureThis mixture was heated
- temperatureto reflux
- customto give a clear yellow solution
- temperaturethe reaction mixture was heated
- temperatureat reflux for 5 hours
- temperaturethe mixture was heated
- temperatureat reflux overnight
- filtrationThe solid was collected by filtration
- washwashed with isopropanol and ethyl acetate
- customdried overnight at ˜40° C. under reduced pressure
出典と根拠
- ORDレコード
- ord-2a5b7e23e3524c69bccccc1f329c4660
- 出典データセット
- uspto-grants-2007_11
- 特許番号
- US07297795B2
関連ノート
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