反応式
[S:1]([NH2:11])(=[O:10])([C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][CH:4]=1)=[O:2].C([NH:20][C:21]#[N:22])(=O)C1C=CC=CC=1>C(O)C.Cl>[S:1]([C:3]1[CH:4]=[CH:5][C:6]([NH:9][C:21]([NH2:22])=[NH:20])=[CH:7][CH:8]=1)(=[O:10])(=[O:2])[NH2:11]参加物
5
実験手順
A mixture of sulphanilamide (20 g, 0.166 mol), benzoyl cyanamide (34 g, 0.33 mmol) in ethanol (60 ml) and concentrated hydrochloric acid (11 ml) was heated on a steam bath until the solvent had evaporated. Water was added and the mixture heated at reflux for 5 minutes. Sodium hydroxide (14.4 g) was added and the mixture heated at reflux. The mixture was allowed to cool and was adjusted to pH2 with hydrochloric acid and the precipitated solid removed by filtration. The filtrate was neutralised and the solvent removed by evaporation. The residue was recrystallized from water to give crude title product. m/z: 215 [MH]+.
後処理
- temperaturewas heated on a steam bath until the solvent
- customhad evaporated
- additionWater was added
- temperaturethe mixture heated
- temperatureat reflux for 5 minutes
- additionSodium hydroxide (14.4 g) was added
- temperaturethe mixture heated
- temperatureat reflux
- temperatureto cool
- customthe precipitated solid removed by filtration
- customthe solvent removed by evaporation
- customThe residue was recrystallized from water
出典と根拠
- ORDレコード
- ord-ee291c72eff94acdb24dbeb334b42ea7
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06855719B1
関連ノート
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