반응식
I[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[CH3:13][C:14]1[O:15][C:16]2[C:22]([NH2:23])=[CH:21][CH:20]=[CH:19][C:17]=2[CH:18]=1.[NH2:24][CH2:25][C:26]1[CH:34]=[CH:33][CH:32]=[C:31]2[C:27]=1[CH:28]=[CH:29][NH:30]2>>[NH:30]1[C:31]2[C:27](=[C:26]([CH2:25][NH:24][C:2]3[C:3]4[CH:4]=[CH:5][C:6]([NH:23][C:22]5[C:16]6[O:15][C:14]([CH3:13])=[CH:18][C:17]=6[CH:19]=[CH:20][CH:21]=5)=[N:7][C:8]=4[CH:9]=[CH:10][CH:11]=3)[CH:34]=[CH:33][CH:32]=2)[CH:28]=[CH:29]1참가 물질
4
실험 절차
The title compound, MS: m/e=419.1 (M+H+), was prepared in accordance with the general method of example 1 from 5-iodo-2-chloroquinoline, (2-methyl-1-benzofuran-7-yl)amine and 4-aminomethylindole.
출처 및 근거
- ORD 기록
- ord-407cd403e32744038291d149148e0964
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07825253B2
연결된 노트
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