反応式
[C:1]([OH:6])(=O)[C:2]([NH2:4])=[O:3].CN1CCOCC1.ClC(OCC)=O.[CH3:20][O:21][C:22]1[CH:23]=[C:24]([CH2:30][CH2:31][NH:32][OH:33])[CH:25]=[CH:26][C:27]=1[O:28][CH3:29].[Cl-].[NH4+]>COCCOC>[CH3:20][O:21][C:22]1[CH:23]=[C:24]([CH2:30][CH2:31][N:32]([OH:33])[C:1]([C:2]([NH2:4])=[O:3])=[O:6])[CH:25]=[CH:26][C:27]=1[O:28][CH3:29]参加物
実験手順
N-[2-(3,4-Dimethoxyphenyl)ethyl]-N-hydroxamide. To a suspension of oxamic acid (195 mg, 2.21 mmol) in 1,2-dimethoxyethane (7 mL) under an argon atmosphere was added dropwise N-methylmorpholine (0.27 mL, 2.42 mmol), followed by ethyl chloroformate (0.23 mL, 2.42 mmol). After stirring for 1 h at room temperature, a solution of N-[2-(3,4-dimethoxyphenyl)ethyl]-N-hydroxyamine (417 mg, 2.10 mmol) in 1,2-dimethoxyethane (5 mL) was added, and the resulting mixture was stirred for 4 h. Saturated aqueous ammonium chloride was added, and the mixture was extracted with methylene chloride (2×). The combined organic extracts were washed successively with 10% hydrochloric acid and water and dried (potassium carbonate). The solvent was removed in vacuo and the residue was purified by flash chromatography, eluting with 5% methanol/methylene chloride, and recrystallized from methanol/methylene chloride to provide the oxamide (98 mg, 17%): m.p. 143°-144° C.
後処理
- stirringthe resulting mixture was stirred for 4 h
- extractionthe mixture was extracted with methylene chloride (2×)
- washThe combined organic extracts were washed successively with 10% hydrochloric acid and water
- dry with materialdried (potassium carbonate)
- customThe solvent was removed in vacuo
- customthe residue was purified by flash chromatography
- washeluting with 5% methanol/methylene chloride
- customrecrystallized from methanol/methylene chloride
出典と根拠
- ORDレコード
- ord-f405f2584e0644dc9937b8412f330290
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05393788
関連ノート
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