Methyl trans-4-chloro-2-(phenylsulfonylamino)cinnamate → HCID 23003564, compound
Reaction equation
[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.Cl[CH2:25][C:26]([C:28]1[O:29][CH:30]=[CH:31][C:32]=1[CH2:33][O:34][CH3:35])=[O:27]>>[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:25]=1[C:26]([C:28]1[O:29][CH:30]=[CH:31][C:32]=1[CH2:33][O:34][CH3:35])=[O:27]Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 57 from methyl trans-4-chloro-2-(penylsulfonylamino)cinnamate (step 1 of Example 8, Method A) and 2-chloroacetyl-3-(methoxymethyl)furan*.
Sources & evidence
- ORD record
- ord-cba221dc2ab94d75b381dc627677be82
- Source dataset
- uspto-grants-2003_08