반응식
[Cl:1][C:2]1[C:3](Cl)=[C:4]2[N:10]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][N:20]4[CH2:25][CH2:24][O:23][CH2:22][CH2:21]4)=[CH:13][CH:12]=3)[NH:8][C:5]2=[N:6][CH:7]=1.[CH2:27]([C:29]1[CH:30]=[C:31]([CH:33]=[CH:34][CH:35]=1)[NH2:32])[CH3:28]>>[Cl:1][C:2]1[C:3]([NH:32][C:31]2[CH:33]=[CH:34][CH:35]=[C:29]([CH2:27][CH3:28])[CH:30]=2)=[C:4]2[NH:10][C:9]([C:11]3[CH:12]=[CH:13][C:14]([O:17][CH2:18][CH2:19][N:20]4[CH2:21][CH2:22][O:23][CH2:24][CH2:25]4)=[CH:15][CH:16]=3)=[N:8][C:5]2=[N:6][CH:7]=1참가 물질
3
실험 절차
By a procedure similar to that of Example 219 but using 6,7-dichloro-2-[4-(2-morpholin-4-ylethoxy)phenyl]-3H-imidazo[4,5-b]pyridine (Example 206) and 3-ethylaniline, the title compound was obtained in 49% yield.
출처 및 근거
- ORD 기록
- ord-99d1697d985e4c11944ec1d9ad6209d5
- 출처 데이터셋
- uspto-grants-2008_08
- 특허 번호
- US07410966B2
연결된 노트
불러오는 중…