반응식
[Cl:1][C:2]1[CH:13]=[CH:12][C:5](/[CH:6]=[CH:7]/[C:8]([O:10][CH3:11])=[O:9])=[C:4]([NH:14]S(C2C=CC=CC=2)(=O)=O)[CH:3]=1.[CH2:24]([O:31][C:32]1[CH:33]=[C:34]([CH:39]=[CH:40][CH:41]=1)[C:35](=[O:38])[CH2:36]Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH3:11][O:10][C:8](=[O:9])[CH2:7][C:6]1[C:5]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:13][CH:12]=2)[NH:14][C:36]=1[C:35](=[O:38])[C:34]1[CH:39]=[CH:40][CH:41]=[C:32]([O:31][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:33]=1참가 물질
3
실험 절차
The title compound was prepared according to the procedure described in Example 57 from methyl trans 4-chloro-2-(phenylsulfonylamino)cinnamate (step 1 of Example 8, Method A) and 3-benzyloxyphenacyl bromide (A. Hernandez et al., J. Org. Chem., 1994, 59, 1058).
출처 및 근거
- ORD 기록
- ord-588122d7a8214075a94e8c6b6134a670
- 출처 데이터셋
- uspto-grants-2003_08
- 특허 번호
- US06608070B1
연결된 노트
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