4-Toluenesulfonyl chloride → 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole
反応式
[NH2:1][C:2]1[N:6]([C:7](=[N:17][OH:18])[C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-:16])=[O:15])[CH:9]=2)[N:5]=[C:4]([CH3:19])[CH:3]=1.C(N(CC)CC)C.[CH3:27][C:28]1[CH:33]=[CH:32][C:31]([S:34](Cl)(=[O:36])=[O:35])=[CH:30][CH:29]=1>C(#N)C>[NH2:1][C:2]1[N:6]([C:7](=[N:17][O:18][S:34]([C:31]2[CH:32]=[CH:33][C:28]([CH3:27])=[CH:29][CH:30]=2)(=[O:36])=[O:35])[C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-:16])=[O:15])[CH:9]=2)[N:5]=[C:4]([CH3:19])[CH:3]=1参加物
実験手順
7.4 g (0.028 mol) of 5-amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole are treated in 90 ml of absolute acetonitrile with 4 ml (0.028 mol) of triethylamine and then, with stirring at room temperature, are treated dropwise with a solution of 5.55 g (0.029 mol) of 4-tosyl chloride in 150 ml of absolute acetonitrile. Stirring is continued for 1 hour and then the mixture is evaporated to dryness. The residue is treated with water and ethyl acetate, the organic phase is washed with water, dried over magnesium sulphate and evaporated under vacuum. The oily residue obtained in this way is crystallised from ethanol. 8.5 g (72%) of 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole with a m. pt. of 156°-158° C. are obtained. The substance is light-sensitive. On recrystallising twice from ethanol, the m. pt. is 165°-169° C.
後処理
- stirringStirring
- customthe mixture is evaporated to dryness
- additionThe residue is treated with water and ethyl acetate
- washthe organic phase is washed with water
- dry with materialdried over magnesium sulphate
- customevaporated under vacuum
- customThe oily residue obtained in this way
- customis crystallised from ethanol
出典と根拠
- ORDレコード
- ord-9e7aea21da4748b6b736179a167e9b9f
- 出典データセット
- uspto-grants-1994_08
- 特許番号
- US05336780
反応ノート
読み込み中…