반응식
[CH3:1][C:2]1[N:6]([CH2:7][CH2:8][CH2:9][NH2:10])[CH:5]=[N:4][CH:3]=1.[CH:11](=[O:18])C1C=CC=CC=1.[CH2:19]([N+]#[C-])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.[O:28]([C:30]#[N:31])[K]>>[CH3:1][C:2]1[N:6]([CH2:7][CH2:8][CH2:9][N:10]2[CH:19]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:30](=[O:28])[NH:31][C:11]2=[O:18])[CH:5]=[N:4][CH:3]=1참가 물질
5
실험 절차
The compound was synthesized starting from (3-(5-methyl-1H-imidazol-1-yl)propyl)amine 0.278 g (2 mmol), benzaldehyde 0.202 ml (2 mmol), benzylisonitrile 0.245 ml (2 mmol) pyridiniumchloride 0.231 g (2 mmol) and KOCN 0.165 g (2 mmol) as described in method 1.
후처리
- customThe compound was synthesized
출처 및 근거
- ORD 기록
- ord-235e2fb653924bcf9c6d9a9eb1844693
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08889709B2
연결된 노트
불러오는 중…