반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([Cl:11])[CH:10]=1)[C:5]([NH2:7])=[O:6].[NH:12]1[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[N:14]=[N:13]1.[C:21]1([CH3:31])[CH:26]=[CH:25][C:24](S(O)(=O)=O)=[CH:23][CH:22]=1>>[N:12]1([CH:3]([NH:7][C:5](=[O:6])[C:4]2[CH:3]=[C:2]([Cl:1])[CH:10]=[C:9]([Cl:11])[CH:8]=2)[C:4]([CH3:8])([CH3:5])[CH2:31][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[N:14]=[N:13]1참가 물질
4
실험 절차
3,5-Dichlorobenzamide, the product from Example 18A, benzotriazole, and p-toluenesulfonic acid were processed as described in Example 18B to provide the title compound.
출처 및 근거
- ORD 기록
- ord-c63d22a4c65143fe90607c29aad576f2
- 출처 데이터셋
- uspto-grants-2002_12
- 특허 번호
- US06495576B2
연결된 노트
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