반응식
[CH3:1][C:2]1[C:18]([CH3:19])=[CH:17][C:5]2[NH:6][C:7]([CH:9]=[CH:10][C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:8][C:4]=2[CH:3]=1.F[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][N:22]=1.N1C=CC=CC=1N1C2C=CC=CC=2N=C1/C=C/C1C=CC=CC=1>>[CH3:19][C:18]1[C:2]([CH3:1])=[CH:3][C:4]2[N:8]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][N:22]=3)[C:7](/[CH:9]=[CH:10]/[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)=[N:6][C:5]=2[CH:17]=1참가 물질
4
실험 절차
The titled compound was prepared from 5,6-dimethyl-2-styryl-1H-benzimidazole and 2-fluoropyridine according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method B).
출처 및 근거
- ORD 기록
- ord-f6aea99db9374e40a962422809ccf227
- 출처 데이터셋
- uspto-grants-2001_10
- 특허 번호
- US06310079B1
연결된 노트
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