반응식
I.[Cl:2][C:3]1[CH:15]=[CH:14][CH:13]=[C:12]([Cl:16])[C:4]=1[CH:5]=[N:6][NH:7][C:8](=[NH:11])SC.[NH2:17][CH2:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1.C(O)C>O>[Cl:2][C:3]1[CH:15]=[CH:14][CH:13]=[C:12]([Cl:16])[C:4]=1[CH:5]=[N:6][NH:7][C:8]([NH:17][CH2:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)=[NH:11]참가 물질
5
실험 절차
A solution of 5.85 g. of methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydriodide and 3.24 g. of 4-(aminomethyl)pyridine in 25 ml. of absolute ethanol is heated under reflux for 24 hours and then diluted with 75 ml. of water, causing the separation of an oil. On standing, the oil crystallizes. Filtration and recrystallization from aqueous ethanol gives the desired product as colorless crystals, m.p. 159°-161° C.
후처리
- temperatureunder reflux for 24 hours
- additiondiluted with 75 ml
- customthe separation of an oil
- customthe oil crystallizes
- filtrationFiltration and recrystallization from aqueous ethanol
출처 및 근거
- ORD 기록
- ord-55aa7ac5eee7444ca5fc4e76b4ff03c6
- 출처 데이터셋
- uspto-grants-1979_05
- 특허 번호
- US04154947
연결된 노트
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