Ethyl orthoformate → 4-bromo-3-methoxyanilino-N-(2,4-dichloro-5-methoxyphenyl)-2-cyano-2-propenamide

HRID 1593770

反応式

HRID 1593770 の反応式
[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

5

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

  1. temperatureThis mixture was heated
  2. temperatureto reflux
  3. customto give a clear yellow solution
  4. temperaturethe reaction mixture was heated
  5. temperatureat reflux for 5 hours
  6. temperaturethe mixture was heated
  7. temperatureat reflux overnight
  8. filtrationThe solid was collected by filtration
  9. washwashed with isopropanol and ethyl acetate
  10. 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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