반응식
[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]참가 물질
5
실험 절차
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]+.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-ee291c72eff94acdb24dbeb334b42ea7
- 출처 데이터셋
- uspto-grants-2005_02
- 특허 번호
- US06855719B1
연결된 노트
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