反応式
[C:1](Cl)(=[O:4])[CH2:2][CH3:3].[NH2:6][C:7]1[N:11]([C:12]2[C:17]([Cl:18])=[CH:16][C:15]([C:19]([F:22])([F:21])[F:20])=[CH:14][C:13]=2[Cl:23])[N:10]=[CH:9][C:8]=1[N:24]1[CH:28]=[N:27][CH:26]=[N:25]1.N1C=CC=CC=1.O>C(#N)C>[Cl:23][C:13]1[CH:14]=[C:15]([C:19]([F:20])([F:22])[F:21])[CH:16]=[C:17]([Cl:18])[C:12]=1[N:11]1[C:7]([NH:6][C:1](=[O:4])[CH2:2][CH3:3])=[C:8]([N:24]2[CH:28]=[N:27][CH:26]=[N:25]2)[CH:9]=[N:10]1参加物
反応条件
- 温度
- 50 °C
実験手順
3.5 g (0.037 mole) of propionyl chloride are added dropwise to a solution of 7.3 g (0.02 mole) of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1,2,4-triazol-1-yl)-pyrazole and 2 g (0.025 mole) of pyridine in 60 ml of acetonitrile, with stirring, and, when the addition has ended, the mixture is stirred at room temperature for a further 12 to 15 hours. For working up, the reaction batch is poured into water and extracted with methylene chloride, the organic phase is washed with water and dried over sodium sulphate and the solvent is removed in vacuo. The residue is dissolved in 100 ml of ethanol, 10 ml of aqueous ammonia are added, the mixture is heated to 50° C. for 15 minutes and concentrated in vacuo and the residue is triturated with water and dried on clay. 6.8 g (81% of theory) of 1-(2,6-dichloro-4-trifluoromethyl-phenyl)-5-propionylamino-4-(1,2,4-triazol-1-yl)-pyrazole of melting point 167° C. to 169° C. are obtained.
後処理
- additionwhen the addition
- stirringthe mixture is stirred at room temperature for a further 12 to 15 hours
- extractionextracted with methylene chloride
- washthe organic phase is washed with water
- dry with materialdried over sodium sulphate
- customthe solvent is removed in vacuo
- dissolutionThe residue is dissolved in 100 ml of ethanol
- addition10 ml of aqueous ammonia are added
- concentrationconcentrated in vacuo
- customthe residue is triturated with water
- customdried on clay
出典と根拠
- ORDレコード
- ord-1b6cce64a360415b9921215c57a9826e
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04614534
関連ノート
読み込み中…